Home NDC 79988-002 Advanced Day Ultimate Protect Sunscreen SPF 50
Product NDC 79988-002
11-digit product format 799880002
Labeler code 79988
Product ID 79988-002_29071920-ba91-871a-e063-6294a90aee27
Type HUMAN OTC DRUG
Nonproprietary name Butyl Methoxydibenzoylmethane, Ethylhexyl Salicylate
Dosage form CREAM
Route TOPICAL
Labeler Medik8 Limited
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-01-06
Substance ETHYLHEXYL SALICYLATE; OCTOCRYLENE; HOMOSALATE; BUTYL METHOXYDIBENZOYLMETHANE
Active strength 4.8; 9.5; 10; 2.8 g/100mL; g/100mL; g/100mL; 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 Advanced Day Ultimate Protect Sunscreen SPF 50
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ETHYLHEXYL SALICYLATE 4.8 g/100mL OCTOCRYLENE 9.5 g/100mL HOMOSALATE 10 g/100mL BUTYL METHOXYDIBENZOYLMETHANE 2.8 g/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 79988-002-05 Advanced Day Ultimate Protect Sunscreen SPF 50 5 mL in 1 BOTTLE CREAM 5 1 79988-002-50 Advanced Day Ultimate Protect Sunscreen SPF 50 50 mL in 1 BOTTLE CREAM 50 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 79988-002 ADVANCED DAY ULTIMATE PROTECT SUNSCREEN SPF 50 (BUTYL METHOXYDIBENZOYLMETHANE, ETHYLHEXYL SALICYLATE) CREAM [MEDIK8 LIMITED] 1 Current NDC, 2 package rows 20250109_29071920-ba90-871a-e063-6294a90aee27.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 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 79988-002-05 79988000205 5 mL in 1 BOTTLE (79988-002-05) 5 ml 2025-01-06 No No Current 79988-002-50 79988000250 50 mL in 1 BOTTLE (79988-002-50) 50 ml 2025-01-06 No No Current