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NDC 87204-248 · HUMAN OTC DRUG · EMULSION

Generic nameOctinoxate 7% Zinc Oxide 5%
Labeler / ManufacturerGuangzhou Huixue Biotechnology Co., Ltd.
Marketing categoryOTC monograph drug · App M020
Dosage form / routeEMULSION · TOPICAL
Active ingredientsOCTINOXATE (.07 mg/30mL)
ZINC OXIDE (.05 mg/30mL)
Marketing started20260715
Marketing ended20270720
Package count1

External sources

Source: openFDA. Public-domain (CC0).