# WHITENING SUNSCREENANTI WRINKLE

NDC: 85819-441
Generic name: WHITENING SUNSCREENANTI WRINKLE
Labeler / Manufacturer: Shantou Oushiya Biotechnology Co.,Ltd
Product type: HUMAN OTC DRUG
Marketing category: UNAPPROVED HOMEOPATHIC
Dosage form: CREAM
Routes: TOPICAL
Marketing started: 20260521



## Active ingredients

- WATER: 52.49 g/1
- TITANIUM DIOXIDE: 8 g/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"85819-441"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=85819-441
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=524384e9-b3f8-4c13-e063-6394a90a8973