Home NDC 87223-001 Zinc Oxide 20%
Product NDC 87223-001
11-digit product format 872230001
Labeler code 87223
Product ID 87223-001_558d3674-3f0c-dcb3-e063-6294a90add44
Type HUMAN OTC DRUG
Nonproprietary name Sunscreen SPF 50
Dosage form LOTION
Route TOPICAL
Labeler The Beach Rooster
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-10-09
Substance ZINC OXIDE
Active strength 20 g/100mL
Pharmacologic classes Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Zinc Oxide 20%
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 20 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SOI2LOH54Z Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 26 of 357 · 7,139 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87223-001-02 87223000102 50 mL in 1 TUBE (87223-001-02) 50 ml 2025-10-09 No No Current