Home NDC 85179-048 Sugargirl SPF 30 Sunscreen Illuminating Stick Sunlight
Product NDC 85179-048
11-digit product format 851790048
Labeler code 85179
Product ID 85179-048_4fab854a-c0ee-1f7b-e063-6394a90a75b1
Type HUMAN OTC DRUG
Nonproprietary name HOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE
Dosage form STICK
Route TOPICAL
Labeler I World LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-12-06
Substance HOMOSALATE; OCTOCRYLENE; OCTISALATE; AVOBENZONE
Active strength 150; 80; 50; 30 mg/g; mg/g; mg/g; mg/g
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 Sugargirl SPF 30 Sunscreen Illuminating Stick Sunlight
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 150 mg/g OCTOCRYLENE 80 mg/g OCTISALATE 50 mg/g AVOBENZONE 30 mg/g
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 Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 85179-048-00 Sugargirl SPF 30 Sunscreen Illuminating Stick Sunlight 10 g in 1 TUBE STICK 10 4
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 85179-048-00 85179004800 10 g in 1 TUBE (85179-048-00) 10 g 2025-12-06 No No Current