得美芙錠食品
得美芙錠食品 : 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
- 1110712402
- Chinese name
- 得美芙錠食品
- English name
- F-FDERMAX COMPLEX TABLETS
- Type
- Imported tablets and capsules
- Published status
- Status not provided in this export; the validity date is shown separately
- Licence holder
- 昌帛實業有限公司
- Registration date
- 2022-06-06
- Published validity end
- 2027-06-06
The foreign register category does not determine the regulatory category of the product in France.
French and European references for recognised ingredients
- À vérifier
The composition lists additive E171 (titanium dioxide), removed from the list of additives allowed in food, supplements included: since 7 August 2022, a supplement containing it can no longer be placed on the market in the Union.
règlement (UE) 2022/63. Regulation (EU) 2022/63: titanium dioxide (E171) removed from the food additives allowed in the EU, retrieved 23 October 2026.
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 |
|---|---|---|
| SILICON HVP CHELATE | SILICON HVP CHELATE | Not identified |
| HYDROLYZED COLLAGEN PEPTIDE(FROM PORCINE SKIN) | HYDROLYZED COLLAGEN PEPTIDE(FROM PORCINE SKIN) | Not identified |
| HAEMATOCOCCUS PLUVIALIS EXTRACT | HAEMATOCOCCUS PLUVIALIS EXTRACT | Not identified |
| NIACINAMIDE ASCORBATE | NIACINAMIDE ASCORBATE | Nicotinamide (vitamine B3) |
| DL-ALPHA TOCOPHERYL ACETATE | DL-ALPHA TOCOPHERYL ACETATE | Vitamine E |
| CORN STARCH | CORN STARCH | Not identified |
| MALTODEXTRIN | MALTODEXTRIN | Maltodextrine |
| SILICON DIOXIDE | SILICON DIOXIDE | Not identified |
| ZINC OXIDE | ZINC OXIDE | Zinc |
| COPPER SULFATE | COPPER SULFATE | Cuivre |
| MAGNESIUM SULFATE | MAGNESIUM SULFATE | Magnésium |
| SODIUM SELENITE | SODIUM SELENITE | Sélénium |
| BORON CITRATE | BORON CITRATE | Bore |
| CALCIUM PHOSPHATE, DIBASIC | CALCIUM PHOSPHATE, DIBASIC | Calcium |
| VITAMIN D3 (CHOLECALCIFEROL) | VITAMIN D3 (CHOLECALCIFEROL) | Vitamine D |
| POWDERED CELLULOSE | POWDERED CELLULOSE | Not identified |
| STEARIC ACID | STEARIC ACID | Acide stéarique |
| CROSS-LINKED SODIUM CARBOXYMETHYL CELLULOSE | CROSS-LINKED SODIUM CARBOXYMETHYL CELLULOSE | Not identified |
| MAGNESIUM STEARATE | MAGNESIUM STEARATE | Not identified |
| HYDROXYPROPYL METHYLCELLULOSE | HYDROXYPROPYL METHYLCELLULOSE | Not identified |
| TITANIUM DIOXIDE | TITANIUM DIOXIDE | Not identified |
| IRON OXIDE YELLOW | IRON OXIDE YELLOW | 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
- 得美芙錠食品
- Active ingredients
- SILICON HVP CHELATE;;HYDROLYZED COLLAGEN PEPTIDE(FROM PORCINE SKIN);;HAEMATOCOCCUS PLUVIALIS EXTRACT;;NIACINAMIDE ASCORBATE;;DL-ALPHA TOCOPHERYL ACETATE;;CORN STARCH;;MALTODEXTRIN;;SILICON DIOXIDE;;ZINC OXIDE;;COPPER SULFATE;;MAGNESIUM SULFATE;;SODIUM SELENITE;;BORON CITRATE;;CALCIUM PHOSPHATE, DIBASIC;;VITAMIN D3 (CHOLECALCIFEROL);;POWDERED CELLULOSE;;STEARIC ACID;;SILICON DIOXIDE;;CROSS-LINKED SODIUM CARBOXYMETHYL CELLULOSE;;MAGNESIUM STEARATE;;HYDROXYPROPYL METHYLCELLULOSE;;TITANIUM DIOXIDE;;IRON OXIDE YELLOW;;
- Valid until
- 1160606
- Registration number
- 1110712402
- Licence holder
- 昌帛實業有限公司
- Registration date
- 1110606
- Published reference
- DHC0B107124023
- Published English name
- F-FDERMAX COMPLEX TABLETS
Official source
View the official register, number 1110712402
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.