唯聖維生素D3 800IU軟膠囊
唯聖維生素D3 800IU軟膠囊 : Product registered in Taiwan. This registration does not constitute authorisation for sale in France or the European Union. It does not demonstrate the safety or efficacy of the product.
TFDA, Taiwan tablets, capsules and medical nutrition registers, retrieved 27 October 2026.
Taiwan Food and Drug Administration (TFDA), Open Government Data License, version 1.0
- Registration number
- 1149088245
- Chinese name
- 唯聖維生素D3 800IU軟膠囊
- English name
- VITAMIN D3 800IU OD SOFTGELS
- Type
- Imported tablets and capsules
- Published status
- Status not provided in this export; the validity date is shown separately
- Licence holder
- 佑康生醫科技有限公司
- Registration date
- 2026-01-15
- Published validity end
- 2031-01-15
The foreign register category does not determine the regulatory category of the product in France.
French and European references for recognised ingredients
No point flagged by the rules applied to recognised ingredients.
Unidentified ingredients are not assessed. The absence of a signal does not establish product compliance.
Published composition
| Published ingredient | Published text and quantity | Identified nutrient or substance |
|---|---|---|
| VITAMIN D3 (CHOLECALCIFEROL) | VITAMIN D3 (CHOLECALCIFEROL) | Vitamine D |
| CORN OIL (GAINED FROM GERMS OF ZEA MAYS L.) | CORN OIL (GAINED FROM GERMS OF ZEA MAYS L.) | Not identified |
| MEDIUM CHAIN TRIGLYCERIDES OIL (FROM FRUIT OF ELAEIS GUINEENSIS L.)) | MEDIUM CHAIN TRIGLYCERIDES OIL (FROM FRUIT OF ELAEIS GUINEENSIS L.)) | Not identified |
| L-MENTHOL | L-MENTHOL | Not identified |
| GRAPEFRUIT FLAVOR | GRAPEFRUIT FLAVOR | Not identified |
| GELATIN | GELATIN | Not identified |
| GLYCEROL | GLYCEROL | Glycérol |
| XYLITOL | XYLITOL | Not identified |
| ERYTHRITOL | ERYTHRITOL | Not identified |
| SUCRALOSE | SUCRALOSE | Not identified |
| ACESULFAME POTASSIUM | ACESULFAME POTASSIUM | Potassium |
| ALLURA RED AC | ALLURA RED AC | Not identified |
The imported data provide no usable daily dosage. No daily dose is estimated and no comparison with dose limits is performed. A published quantity may refer to a preparation or an unspecified unit. Chinese names are retained without translation.
Original register data
View published fields and their variants
- Product name
- 唯聖維生素D3 800IU軟膠囊
- Active ingredients
- VITAMIN D3 (CHOLECALCIFEROL);;VITAMIN D3 (CHOLECALCIFEROL);;CORN OIL (GAINED FROM GERMS OF ZEA MAYS L.);;MEDIUM CHAIN TRIGLYCERIDES OIL (FROM FRUIT OF ELAEIS GUINEENSIS L.));;L-MENTHOL;;GRAPEFRUIT FLAVOR;;GELATIN;;GLYCEROL;;XYLITOL;;ERYTHRITOL;;SUCRALOSE;;ACESULFAME POTASSIUM;;ALLURA RED AC;;
- Valid until
- 1200115
- Registration number
- 1149088245
- Licence holder
- 佑康生醫科技有限公司
- Registration date
- 1150115
- Published reference
- DHC0B490882458
- Published English name
- VITAMIN D3 800IU OD SOFTGELS
Official source
View the official register, number 1149088245
Taiwan Food and Drug Administration (TFDA), Open Government Data License, version 1.0
Open Government Data License, version 1.0
Official warnings (Health Canada)
Health Canada publishes warnings on these ingredients:
- VITAMIN D3 (CHOLECALCIFEROL)
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).
They concern the ingredient, not this product or its dose. They do not replace medical advice.
The evidence date of this ingredient list is unknown.
Has the product changed? Photograph the packaging.
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.