Home NDC 85739-004 Tallow Sunscreen SPF 30
Product NDC 85739-004
11-digit product format 857390004
Labeler code 85739
Product ID 85739-004_3b410ed7-c62a-e39c-e063-6294a90a12f6
Type HUMAN OTC DRUG
Nonproprietary name Non-Nano Zinc Oxide 19%
Dosage form CREAM
Route TOPICAL
Labeler FOUNDATION COMMERCE INC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-08-25
Substance ZINC OXIDE
Active strength 19 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 Tallow Sunscreen SPF 30
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 19 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 85739-004-01 Tallow Sunscreen SPF 30 100 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 85739-004-01 85739000401 100 mL in 1 CARTON (85739-004-01) 100 ml 2025-08-25 No No Current