Home NDC 87458-003 UV DEFENSE FACE MINERAL SPF 50
Product NDC 87458-003
11-digit product format 874580003
Labeler code 87458
Product ID 87458-003_4bc4d94a-d4e6-7baa-e063-6394a90a2487
Type HUMAN OTC DRUG
Nonproprietary name ZINC OXIDE
Dosage form LOTION
Route TOPICAL
Labeler BETTER INVENTION LTD
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-02-25
Substance ZINC OXIDE
Active strength 17.88 mg/100mL
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 UV DEFENSE FACE MINERAL SPF 50
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 17.88 mg/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.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 87458-003-01 UV DEFENSE FACE MINERAL SPF 50 1 in 1 CARTON LOTION 1 2 87458-003-01 UV DEFENSE FACE MINERAL SPF 50 40 mL in 1 TUBE LOTION 40 2
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 87458-003-01 87458000301 1 TUBE in 1 CARTON (87458-003-01) / 40 mL in 1 TUBE 1 tube 2026-02-25 No No Current