Home NDC 87092-004 Tallow and SolSUNSCREEN SPF50
Product NDC 87092-004
11-digit product format 870920004
Labeler code 87092
Product ID 87092-004_52cb56cf-f093-9f86-e063-6394a90ac2d3
Type HUMAN OTC DRUG
Nonproprietary name Non-Nano Zinc Oxide 25%
Dosage form CREAM
Route CUTANEOUS
Labeler Guangzhou Shengyanghui Industrial Trading Co., Ltd
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-05-28
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 Tallow and SolSUNSCREEN SPF50
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.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 87092-004-01 Tallow and SolSUNSCREEN SPF50 1 g in 1 TUBE CREAM 1 1 87092-004-02 Tallow and SolSUNSCREEN SPF50 1 in 1 BOX CREAM 1 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 27 of 354 · 7,077 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87092-004-01 87092000401 1 g in 1 TUBE 1 g Historical 87092-004-02 87092000402 1 TUBE in 1 BOX (87092-004-02) / 1 g in 1 TUBE (87092-004-01) 1 tube 2026-05-28 No No Current