# MENS SPF50 ALL IN ONE SUNSCREEN

NDC: 87593-101
Generic name: MENS SPF50 ALL IN ONE SUNSCREEN
Labeler / Manufacturer: Lance (Guangzhou) Biological Technology Co., Ltd.
Product type: HUMAN OTC DRUG
Marketing category: OTC monograph drug
Dosage form: CREAM
Routes: CUTANEOUS
Marketing started: 20260720

FDA application: M020

## Active ingredients

- HOMOSALATE: 4.9 g/50g
- OCTISALATE: 2.5 g/50g
- ZINC OXIDE: 6 g/50g
- TITANIUM DIOXIDE: 2 g/50g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"87593-101"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=87593-101
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=57074480-77fd-cc06-e063-6294a90a28d4