Home NDC 60771-0050 MELAO TALLOW SUNSCREEN
Product NDC 60771-0050
11-digit product format 607710050
Labeler code 60771
Product ID 60771-0050_519d9f52-b705-d6cd-e063-6294a90a6e42
Type HUMAN OTC DRUG
Nonproprietary name ETHYLHEXYL METHOXYCINNAMATA,ETHYLHEXYL SALICYATE
Dosage form CREAM
Route TOPICAL
Labeler Guangzhou Haishi Biological Technology Co., Ltd.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-05-13
Substance ETHYLHEXYL METHOXYCINNAMATE; ETHYLHEXYL SALICYLATE
Active strength 4; 4 g/100g; 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 MELAO TALLOW SUNSCREEN
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ETHYLHEXYL METHOXYCINNAMATE 4 g/100g ETHYLHEXYL SALICYLATE 4 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4Y5P7MUD51 Internal UNII lookup 4X49Y0596W 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 60771-0050-1 MELAO TALLOW SUNSCREEN 60 g in 1 JAR CREAM 60 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 60771-0050-1 60771005001 60 g in 1 JAR (60771-0050-1) 60 g 2026-05-13 No No Current