Home NDC 87604-002 FORGESKIN
Product NDC 87604-002
11-digit product format 876040002
Labeler code 87604
Product ID 87604-002_4fe910d0-b00d-da16-e063-6294a90ac999
Type HUMAN OTC DRUG
Nonproprietary name MINERAL TALLOW SUNSCREEN
Dosage form CREAM
Route CUTANEOUS
Labeler GUANGZHOU KANGLIXIN BIOTECHNOLOGY CO.,LTD
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-04-20
Substance ZINC OXIDE
Active strength 250 mg/mL
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 FORGESKIN
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 250 mg/mL
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 87604-002-01 FORGESKIN 80 mL in 1 BOTTLE CREAM 80 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 242 of 353 · 7,041 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87604-002-01 87604000201 80 mL in 1 BOTTLE (87604-002-01) 80 ml 2026-04-20 No No Current