Other
Drug Facts
SHISEIDO AMERICA INC.
NEW YORK, N.Y. 10022
SHISEIDO DIST.
NEW YORK • PARIS • MILANO
The following Structured Product Label (SPL) was submitted to the FDA by Shiseido Americas Corporation for the product Shiseido Benefiance Nutriperfect Day (NDC 58411-351). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding other, otc - purpose, uses, otc - do not use, otc - when using, otc - stop use, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Drug Facts
SHISEIDO AMERICA INC.
NEW YORK, N.Y. 10022
SHISEIDO DIST.
NEW YORK • PARIS • MILANO
| ACTIVE INGREDIENTS: | Purpose |
|---|---|
| AVOBENZONE 2.5% | Sunscreen |
| OCTINOXATE 7.4% | Sunscreen |
| OCTOCRYLENE 2.0% | Sunscreen |
For external use only
Do not use on damaged or broken skin
When using this product keep out of eyes. Rinse with water to remove.
Stop use and ask a doctor if rash occurs
Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.
For sunscreen use:
WATER, BUTYLENE GLYCOL, GLYCERIN, DIPROPYLENE GLYCOL, DIMETHICONE, GLYCERYL STEARATE SE, BEHENYL ALCOHOL, PEG/PPG-14/7 DIMETHYL ETHER, POLYBUTYLENE GLYCOL/PPG-9/1 COPOLYMER, HYDROGENATED POLYDECENE, ISOPROPYL MYRISTATE, MYRISTYL MYRISTATE, MICROCRYSTALLINE WAX, PEG-40 STEARATE, SILICA, CARNOSINE, XANTHAN GUM, ERYTHRITOL, TOCOPHERYL ACETATE, POTASSIUM ASCORBYL TOCOPHERYL PHOSPHATE, PANTHENYL ETHYL ETHER, SODIUM ACETYLATED HYALURONATE, SORBITAN TRISTEARATE, STEARYL ALCOHOL, CELLULOSE GUM, SODIUM METAPHOSPHATE, TRISODIUM EDTA, BHT, SODIUM METABISULFITE, TOCOPHEROL, PHENOXYETHANOL, FRAGRANCE, IRON OXIDES,
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