Home NDC 85739-005 Kids Tallow Sunscreen SPF50
Product NDC 85739-005
11-digit product format 857390005
Labeler code 85739
Product ID 85739-005_3b4eca91-9660-66c6-e063-6394a90a78ca
Type HUMAN OTC DRUG
Nonproprietary name Non-Nano Zinc Oxide 25%
Dosage form CREAM
Route TOPICAL
Labeler FOUNDATION COMMERCE INC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-08-26
Substance ZINC OXIDE
Active strength 25 g/100mL
NDC exclude flag No
Listing certified through 2026-12-31
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 Kids Tallow Sunscreen SPF50
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 25 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.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 85739-005-01 Kids Tallow Sunscreen SPF50 100 mL in 1 CARTON CREAM 100 1
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 85739-005-01 85739000501 100 mL in 1 CARTON (85739-005-01) 100 ml 2025-08-26 No No Current