Home NDC 84066-105 Absolut Skin SPF 50 Moisturizing Sunscreen
Product NDC 84066-105
11-digit product format 840660105
Labeler code 84066
Product ID 84066-105_46874227-b3d7-a1fb-e063-6394a90a3101
Type HUMAN OTC DRUG
Nonproprietary name ETHYLHEXYL METHOXYCINNAMATE,ETHYLHEXYL SALICYLATE,METHYLENE BIS-BENZOTRIAZOLYL TETRAMETHYLBUTYLPHENOL,OCTOCRYLENE
Dosage form CREAM
Route TOPICAL
Labeler Guangzhou Tata Biotechnology Co., Ltd.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-04-10
Substance METHYLENE BIS-BENZOTRIAZOLYL TETRAMETHYLBUTYLPHENOL; OCTOCRYLENE; ETHYLHEXYL METHOXYCINNAMATE; ETHYLHEXYL SALICYLATE
Active strength 2.5; 2; 5; 3 mg/100mL; mg/100mL; mg/100mL; mg/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 Absolut Skin SPF 50 Moisturizing Sunscreen
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength METHYLENE BIS-BENZOTRIAZOLYL TETRAMETHYLBUTYLPHENOL 2.5 mg/100mL OCTOCRYLENE 2 mg/100mL ETHYLHEXYL METHOXYCINNAMATE 5 mg/100mL ETHYLHEXYL SALICYLATE 3 mg/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 84066-105-01 Absolut Skin SPF 50 Moisturizing Sunscreen 50 mL in 1 BOTTLE CREAM 50 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 84066-105 ABSOLUT SKIN SPF 50 MOISTURIZING SUNSCREEN (ETHYLHEXYL METHOXYCINNAMATE,ETHYLHEXYL SALICYLATE,METHYLENE BIS-BENZOTRIAZOLYL TETRAMETHYLBUTYLPHENOL,OCTOCRYLENE) CREAM [GUANGZHOU TATA BIOLOGICAL TECHNOLOGY CO., LTD.] 1 Current NDC, 1 package rows 20250423_3264543c-e8f5-da9a-e063-6394a90ac8c6.zip
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 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 84066-105-01 84066010501 50 mL in 1 BOTTLE (84066-105-01) 50 ml 2025-04-10 No No Current