Instaflex Joint Health
Retirée du marché américain le 16 June 2025 (selon le DSLD)
Instaflex, food supplement from the US market
Label withdrawn from the US market. Instaflex Joint Health (Instaflex), a food supplement au code-barres 855710002000, is described by its US market label, recorded on 18 July 2023. If sold in France, it would be subject to 2 points of French or European regulation, detailed below. The formula sold in Europe under the same name may differ.
Official label, entered on 18 July 2023. 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
- Dose déclarée au-delà d'une limite
Potassium: up to 176 mg a day according to the label (at most 1 serving a day), above the maximum dose of 80 mg set in France for a food supplement (2006 Order, not revised since November 2006).
Source: French orders of 9 May 2006 and 14 November 2006 as published in the Official Journal (maximum daily doses), arrêté du 9 mai 2006, annexe III.
- Conditions légales
Salix alba L.: L'étiquetage doit comporter un avertissement déconseillant l'emploi aux personnes souffrant d'allergie aux dérivés salicylés.
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
- Instaflex
- Barcode
- 855710002000
- Form
- Capsule
- One serving
- 3 capsules
- Servings
- up to 1 serving per day
- Other ingredients (in English, as written)
- Gelatin
| Ingredient (as written, in English) | Category | Per serving |
|---|---|---|
| Chloride | Mineral | 177 mg |
| Potassium | Mineral | 176 mg |
| Glucosamine Sulfate 2KCl | Other substance | 1,500 mg |
| Methylsulfonylmethane | Other substance | 500 mg |
| White Willow Bark Extract (Salix alba) | Plant | 250 mg |
| Ginger root extract | Plant | 250 mg |
| Boswellia serrata Resin Extract (Boswellia serrata) | Plant | 125 mg |
| Turmeric Root Extract (Curcuma longa) | Plant | 50 mg |
| Cayenne (Capsicum annuum) | Plant | 50 mg |
| Hyaluronic Acid | Other substance | 4 mg |
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.
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: Instaflex Joint Health
Entered into DSLD on 25 June 2018. Retirée du marché américain le 4 May 2022 (selon le DSLD).- Same quantity, different name: Boswellia serrata extract in this version; Boswellia serrata Resin Extract on the displayed label (125 mg)
Official label: Instaflex Joint Support
Entered into DSLD on 26 August 2014. Retirée du marché américain le 19 January 2018 (selon le DSLD).- Active ingredient removed : Chloride (177 mg)
- Active ingredient removed : Potassium (176 mg)
- Same quantity, different name: Boswellia serrata extract in this version; Boswellia serrata Resin Extract on the displayed label (125 mg)
- Same quantity, different name: Glucosamine Sulfate in this version; Glucosamine Sulfate 2KCl on the displayed label (1,500 mg)
Official label: Instaflex Joint Support
Entered into DSLD on 25 March 2013. Retirée du marché américain le 6 March 2013 (selon le DSLD).- Active ingredient removed : Chloride (177 mg)
- Active ingredient removed : Potassium (176 mg)
- Same quantity, different name: Boswellia serrata extract in this version; Boswellia serrata Resin Extract on the displayed label (125 mg)
- Same quantity, different name: Glucosamine Sulfate in this version; Glucosamine Sulfate 2KCl on the displayed label (1,500 mg)
- Same quantity, different name: MSM in this version; Methylsulfonylmethane on the displayed label (500 mg)
- Same quantity, different name: Turmeric Extract 25:1 in this version; Turmeric Root Extract on the displayed label (50 mg)
Official label: Instaflex Joint Support
Entered into DSLD on 25 November 2011. Retirée du marché américain le 31 July 2014 (selon le DSLD).- Active ingredient added : Glucosamine Sulfate (1,250 mg)
- Active ingredient removed : Chloride (177 mg)
- Active ingredient removed : Glucosamine Sulfate 2KCl (1,500 mg)
- Active ingredient removed : Potassium (176 mg)
- Same quantity, different name: Boswella Serrata Extract in this version; Boswellia serrata Resin Extract on the displayed label (125 mg)
- Same quantity, different name: Ginger root concentrate in this version; Ginger root extract on the displayed label (250 mg)
Source
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.
List declared on (register: Dietary Supplement Label Database (DSLD), US National Institutes of Health: current and off-market labels).
List recorded in 2023. Photograph the packaging to check whether it has changed. Photograph the packaging
Brand : Instaflex