Home NDC 87952-003 Utu Hydrating Sun Balm Broad Spectrum SPF 50
Product NDC 87952-003
11-digit product format 879520003
Labeler code 87952
Product ID 87952-003_5a202afd-9ad5-f139-e063-6394a90aaefb
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide
Dosage form OINTMENT
Route TOPICAL
Labeler Utu Co
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-09-25
Substance ZINC OXIDE
Active strength 25 g/100g
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 Utu Hydrating Sun Balm Broad Spectrum SPF 50
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 25 g/100g
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 87952-003-03 87952000303 1 BOX in 1 BOX (87952-003-03) / 1 CAN in 1 BOX (87952-003-02) / 28 g in 1 CAN (87952-003-01) 1 box 2024-09-25 No No Current