Prosvent Ultra Blend
En vente sur le marché américain (selon le DSLD)
Prosvent, food supplement from the US market
Prosvent Ultra Blend (Prosvent), a food supplement au code-barres 874617006997, is described by its US market label. If sold in France, it would be subject to 3 points of French or European regulation, detailed below. The formula sold in Europe under the same name may differ.
Official label. Dietary Supplement Label Database (DSLD), US National Institutes of Health: current and off-market labels, retrieved 27 October 2026.
Source: NIH Office of Dietary Supplements, Dietary Supplement Label Database (CC0); US market labels.
Displayed label: Official label. Labels on the market are prioritised, followed by the most recent for the same status.
If this product were sold in France
- Conditions légales
Urtica dioica L.: L'étiquetage des compléments alimentaires contenant les parties souterraines de cette plante doit comporter une mention recommandant de prendre conseil auprès d'un professionnel de santé ("Demander l'avis de votre médecin et /ou pharmacien").
Source: French orders of 9 May 2006 (nutrients), 24 June 2014 (plants) and 26 September 2016 (other substances), consolidated LEGI collection, arrêté du 24 juin 2014, annexe I.
- Conditions légales
Serenoa repens (W.Bartram) Small: L'étiquetage doit comporter une mention recommandant de prendre conseil auprès d'un professionnel de santé ("Demander l'avis de votre médecin et /ou pharmacien").
Source: French orders of 9 May 2006 (nutrients), 24 June 2014 (plants) and 26 September 2016 (other substances), consolidated LEGI collection, arrêté du 24 juin 2014, annexe I.
- Conditions légales
Prunus africana (Hook. f.) Kalkman: L'étiquetage doit comporter une mention recommandant de prendre conseil auprès d'un professionnel de santé.
Source: French orders of 9 May 2006 (nutrients), 24 June 2014 (plants) and 26 September 2016 (other substances), consolidated LEGI collection, arrêté du 24 juin 2014, annexe I.
A daily dose is calculated only if the label gives the maximum number of servings and a unit of mass (or international units for vitamin D). Quantities come from the label, not an analysis. In the United States, the label presents this product as a ‘dietary supplement’; in France, a product of this type may belong to another category (a sports powder, for example), and maximum food supplement doses do not apply to it.
Label composition
- Brand
- Prosvent
- Barcode
- 874617006997
- Form
- Capsule
- One serving
- 1 capsule
- Servings
- up to 2 servings per day
- Other ingredients (in English, as written)
- Hydroxypropyl Methylcellulose, Stearic Acid, Silica, Starch, modified Food Starch, Rice concentrate
| Ingredient (as written, in English) | Category | Per serving |
|---|---|---|
| Vitamin D3 | Vitamin | 2.5 µg |
| Zinc | Mineral | 5 mg |
| Cranberry fruit powder | Plant | 250 mg |
| Lycopene | Other substance | 1 mg |
| Black Pepper fruit extract (Piper nigrum) | Plant | 1 mg |
| Proprietary Blend | Blend | 310.6 mg |
| Stinging Nettle root extract (Urtica dioica) | Plant | not stated |
| Mixed Plant Sterols | Fat | not stated |
| Pumpkin seed extract (Cucurbita pepo) | Plant | not stated |
| Saw Palmetto fruit extract (Serenoa repens) | Plant | not stated |
| Pygeum bark extract (Prunus africana) | Plant | not stated |
Other versions of this label
The differences below describe each other version relative to the label shown on this page. They concern active ingredient rows and quantities per serving as written. Missing quantities are not estimated and different units are not converted. Dates refer to entry into DSLD, not necessarily to a formula change.
Official label: Perfect Omega
Entered into DSLD on 22 November 2022. En vente sur le marché américain (selon le DSLD).- Active ingredient added : Calories (10 Calorie(s))
- Active ingredient added : Docosahexaenoic Acid (383 mg)
- Active ingredient added : Eicosapentaenoic Acid (510 mg)
- Active ingredient added : Total EPA + DHA (893 mg)
- Active ingredient added : Total Fat (1.5 Gram(s))
- Active ingredient added : Total Omega-3 Fatty Acids (956 mg)
- Active ingredient removed : Black Pepper fruit extract (1 mg)
- Active ingredient removed : Cranberry fruit powder (250 mg)
- Active ingredient removed : Lycopene (1 mg)
- Active ingredient removed : Mixed Plant Sterols (quantity not stated)
- Active ingredient removed : Proprietary Blend (310.6 mg)
- Active ingredient removed : Pumpkin seed extract (quantity not stated)
- Active ingredient removed : Pygeum bark extract (quantity not stated)
- Active ingredient removed : Saw Palmetto fruit extract (quantity not stated)
- Active ingredient removed : Stinging Nettle root extract (quantity not stated)
- Active ingredient removed : Vitamin D3 (2.5 mcg)
- Active ingredient removed : Zinc (5 mg)
Official label: Prosvent
Entered into DSLD on 22 November 2022. Retirée du marché américain le 18 January 2022 (selon le DSLD).- Active ingredient removed : Cranberry fruit powder (250 mg)
- Same quantity, different name: Pumpkin Seed Oil Extract in this version; Pumpkin seed extract on the displayed label (quantity not stated)
Official label: Prosvent Ultra Blend
Entered into DSLD on 24 October 2022. Retirée du marché américain le 17 June 2022 (selon le DSLD).- Same quantity, different name: BioPerine in this version; Black Pepper fruit extract on the displayed label (1 mg)
- Same quantity, different name: Pygeum africanum Bark Extract in this version; Pygeum bark extract on the displayed label (quantity not stated)
Official label: Prosvent Ultra Blend
Entered into DSLD on 22 January 2021. Retirée du marché américain le 16 October 2020 (selon le DSLD).Same active composition.
Official label: Prosvent
Entered into DSLD on 22 January 2021. En vente sur le marché américain (selon le DSLD).- Active ingredient added : Nettle root extract (quantity not stated)
- Active ingredient added : Pumpkin Seed Oil Extract (quantity not stated)
- Active ingredient removed : Cranberry fruit powder (250 mg)
- Active ingredient removed : Pumpkin seed extract (quantity not stated)
- Active ingredient removed : Stinging Nettle root extract (quantity not stated)
Official label: Prosvent
Entered into DSLD on 22 December 2019. Retirée du marché américain le 16 October 2020 (selon le DSLD).- Active ingredient added : Nettle root extract (quantity not stated)
- Active ingredient added : Pumpkin Seed Oil Extract (quantity not stated)
- Active ingredient added : Pygeum africanum extract (quantity not stated)
- Active ingredient added : Saw Palmetto extract (quantity not stated)
- Active ingredient added : Sterol Esters (quantity not stated)
- Active ingredient removed : Cranberry fruit powder (250 mg)
- Active ingredient removed : Mixed Plant Sterols (quantity not stated)
- Active ingredient removed : Pumpkin seed extract (quantity not stated)
- Active ingredient removed : Pygeum bark extract (quantity not stated)
- Active ingredient removed : Saw Palmetto fruit extract (quantity not stated)
- Active ingredient removed : Stinging Nettle root extract (quantity not stated)
- Same quantity, different name: Black Pepper extract in this version; Black Pepper fruit extract on the displayed label (1 mg)
- Different quantity per serving : Proprietary Blend: 355 mg in this version; 310.6 mg on the displayed label
- Different unit, without conversion : Lycopene: quantity not stated in this version; 1 mg on the displayed label
- Different unit, without conversion : Vitamin D3: 100 IU in this version; 2.5 mcg on the displayed label
This information reproduces the US label recorded by the US National Institutes of Health (NIH). It does not say whether the product is effective and does not replace advice from a doctor or pharmacist, particularly during pregnancy or when taking medication.
Official warnings (Health Canada)
Health Canada publishes warnings on these ingredients:
- Vitamin D3
Read the warning, when it applies and the studies cited
VITAMIN D (>1,000 - 2,500 IU)
Route of administration: Oral
Cautions and warnings
Condition of application: All products except products containing zinc sourced from picolinate requiring a contraindication.
Ask a health care practitioner/health care provider/health care professional/doctor/physician before use if you are pregnant or breastfeeding.
Condition of application: All products.
Ask a health care practitioner/health care provider/health care professional/doctor/physician before use if you have kidney disorders (NIH 2024; BfR 2020).
2 studies cited in the text have no matching reference in the monograph (see the anomalies listed on the sources page).
Ask a health care practitioner/health care provider/health care professional/doctor/physician before use if you are taking other supplements or products containing vitamin D or vitamin D analogues.
Ask a health care practitioner/health care provider/health care professional/doctor/physician before use if you are taking any medications including antacids, anticonvulsants, digoxin, cholestyramine, colestipol, mineral oil, steroids, statins or thiazide diuretics (NNHPD 2021; BfR 2020).
2 studies cited in the text have no matching reference in the monograph (see the anomalies listed on the sources page).
Ask a health care practitioner/health care provider/health care professional/doctor/physician before use to determine if you would benefit from additional vitamin D as 15-20 mcg (600-800 IU) of vitamin D per day is an adequate quantity for most individuals.
Applies to products containing vitamin K2.
Ask a health care practitioner/health care provider/health care professional/doctor/physician before use if you are taking blood thinners (NNHPD 2026).
1 study cited in the text has no matching reference in the monograph (see the anomalies listed on the sources page).
Applies to products providing 25-34 mg of zinc per day for adults 18 years or 31-50 mg of zinc per day for adults 19 years and older.
Ask a health care practitioner/health care provider/health care professional/doctor/physician before use if you are unsure whether you are taking enough copper as zinc supplementation can cause a copper deficiency (NNHPD 2026).
1 study cited in the text has no matching reference in the monograph (see the anomalies listed on the sources page).
Contraindications
Condition of application: All products.
Do not use if you have hypercalcemia and/or hypercalciuria (NIH 2024; BfR 2020).
2 studies cited in the text have no matching reference in the monograph (see the anomalies listed on the sources page).
Applies to products containing zinc sourced from picolinate.
Do not use if you are pregnant or breastfeeding (NNHPD 2026).
1 study cited in the text has no matching reference in the monograph (see the anomalies listed on the sources page).
Known adverse reactions
Condition of application: All products.
Stop use and ask a health care practitioner/health care provider/health care professional/doctor/physician if the following early symptoms of hypercalcemia occur: weakness, fatigue, drowsiness, headache, lack of appetite, dry mouth, metallic taste, nausea, vomiting, vertigo, ringing in the ears, lack of coordination and muscle weakness or if you develop any other symptom (NIH 2024; BfR 2020).
2 studies cited in the text have no matching reference in the monograph (see the anomalies listed on the sources page).
Applies to products providing more than 350 mg of magnesium per day.
When using this product you may experience diarrhea (NNHPD 2026).
1 study cited in the text has no matching reference in the monograph (see the anomalies listed on the sources page).
- Stinging Nettle root extract
Read the warning, when it applies and the studies cited
STINGING NETTLE JUICE
Route of administration: Oral
Cautions and warnings
Condition of application: All products except nutritive tonics.
Ask a health care practitioner/health care provider/health care professional/doctor/physician if symptoms persist or worsen.
Contraindications
Do not use if you are pregnant or breastfeeding (Brinker 2010; Barnes et al. 2007; Tilgner 1999).
3 studies cited in the text have no matching reference in the monograph (see the anomalies listed on the sources page).
Known adverse reactions
Condition of application: All products except those making only a diuretic claim*.
When using this product diuretic effect may occur.
*Note: This statement can be removed from the label if a diuretic claim is included.
Health Canada monograph dated 27 March 2026
STINGING NETTLE - URTICA DIOICA
Route of administration: Oral
Cautions and warnings
Condition of application: All products except nutritive tonics.
Ask a health care practitioner/health care provider/health care professional/doctor/physician if symptoms persist or worsen.
Contraindications
Do not use if you are pregnant or breastfeeding (Brinker 2010; Barnes et al. 2007; Tilgner 1999).
3 studies cited in the text have no matching reference in the monograph (see the anomalies listed on the sources page).
Known adverse reactions
All products except those making only a diuretic claim*
When using this product diuretic effect may occur.
*Note: This statement can be removed from the label if a diuretic claim is included.
- Saw Palmetto fruit extract
Read the warning, when it applies and the studies cited
SAW PALMETTO – SERENOA REPENS
Route of administration: Oral
Cautions and warnings
Condition of application: All subpopulations.
Ask a health care practitioner/health care provider/health care professional/doctor/physician if symptoms persist or worsen.
Condition of application: Adult males only.
Ask a health care practitioner/health care provider/health care professional/doctor/physician before use to exclude a diagnosis of prostate cancer (USP-NF 2024; Mills and Bone 2005).
2 studies cited in the text have no matching reference in the monograph (see the anomalies listed on the sources page).
Condition of application: Adult females only.
Ask a health care practitioner/health care provider/health care professional/doctor/physician before use if you are taking oral contraceptives or hormone replacement therapy (UpToDate 2024).
1 study cited in the text has no matching reference in the monograph (see the anomalies listed on the sources page).
Contraindications
Condition of application: Adult females only.
Do not use if you are pregnant, breastfeeding, or attempting to conceive (UpToDate 2024).
1 study cited in the text has no matching reference in the monograph (see the anomalies listed on the sources page).
- Pygeum bark extract
Read the warning, when it applies and the studies cited
PYGEUM - PRUNUS AFRICANA
Route of administration: Oral
Cautions and warnings
Condition of application: Standardized extracts making a claim for symptoms of benign prostatic hyperplasia (adult males).
Ask a health care practitioner/health care provider/health care professional/doctor/physician if symptoms persist or worsen.
Ask a health care practitioner/health care provider/health care professional/doctor/physician before use to exclude a diagnosis of prostate cancer (Goldman and Ausiello 2004).
1 study cited in the text has no matching reference in the monograph (see the anomalies listed on the sources page).
Condition of application: Non-standardized preparations for adults (i.e., including women) (safety only).
Ask a health care practitioner/health care provider/health care professional/doctor/physician before use if you are pregnant or breastfeeding.
They concern the ingredient, not this product or its dose. They do not replace medical advice.
List declared on (register: Dietary Supplement Label Database (DSLD), US National Institutes of Health: current and off-market labels).
Brand : Prosvent
Is something on this product wrong or out of date, whether you are a reader or the brand? Write to contact@compoatlas.com: every correction is published in the corrections log.