生物素5000MCG+鈣錠
生物素5000MCG+鈣錠 : 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
- 1159034624
- Chinese name
- 生物素5000MCG+鈣錠
- English name
- ULTRA BIOTIN 5000 MCG TABLET
- Type
- Imported tablets and capsules
- Published status
- Status not provided in this export; the validity date is shown separately
- Licence holder
- 日落恩賜國際有限公司
- Registration date
- 2026-05-27
- Published validity end
- 2031-05-27
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 |
|---|---|---|
| BIOTIN | BIOTIN | Biotine (vitamine B8) |
| CALCIUM PHOSPHATE，DIBASIC | CALCIUM PHOSPHATE，DIBASIC | Calcium |
| MICROCRYSTALLINE α-CELLULOSE | MICROCRYSTALLINE α-CELLULOSE | Not identified |
| CROSS-LINKED SODIUM CARBOXYMETHYL CELLULOSE | CROSS-LINKED SODIUM CARBOXYMETHYL CELLULOSE | Not identified |
| MAGNESIUM STEARATE | MAGNESIUM STEARATE | Not identified |
| STEARIC ACID | STEARIC ACID | Acide stéarique |
| SILICON DIOXIDE | SILICON DIOXIDE | 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
- 生物素5000MCG+鈣錠
- Active ingredients
- BIOTIN;;CALCIUM PHOSPHATE，DIBASIC;;MICROCRYSTALLINE α-CELLULOSE;;CROSS-LINKED SODIUM CARBOXYMETHYL CELLULOSE;;MAGNESIUM STEARATE;;STEARIC ACID;;SILICON DIOXIDE;;
- Valid until
- 1200527
- Registration number
- 1159034624
- Licence holder
- 日落恩賜國際有限公司
- Registration date
- 1150527
- Published reference
- DHC0B590346248
- Published English name
- ULTRA BIOTIN 5000 MCG TABLET
Official source
View the official register, number 1159034624
Taiwan Food and Drug Administration (TFDA), Open Government Data License, version 1.0
Open Government Data License, version 1.0
The evidence date of this ingredient list is unknown.
Has the product changed? Photograph the packaging.