Home NDC 85179-028 Poolside Orange Creme SPF 30 Scented Sunscreen
Product NDC 85179-028
11-digit product format 851790028
Labeler code 85179
Product ID 85179-028_47f8ec86-f556-b0b3-e063-6294a90a4c89
Type HUMAN OTC DRUG
Nonproprietary name HOMOSALATE, OCTOCRYLENE, OCTISALATE, OCTINOXATE, AVOBENZONE
Dosage form LIQUID
Route TOPICAL
Labeler I World LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-12-17
Substance HOMOSALATE; OCTOCRYLENE; OCTISALATE; OCTINOXATE; AVOBENZONE
Active strength 100; 80; 50; 50; 30 mg/mL; mg/mL; mg/mL; mg/mL; 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 Poolside Orange Creme SPF 30 Scented Sunscreen
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 100 mg/mL OCTOCRYLENE 80 mg/mL OCTISALATE 50 mg/mL OCTINOXATE 50 mg/mL AVOBENZONE 30 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 5 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 85179-028-00 Poolside Orange Creme SPF 30 Scented Sunscreen 95 mL in 1 TUBE LIQUID 95 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 238 of 346 · 6,912 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 85179-028-00 85179002800 95 mL in 1 TUBE (85179-028-00) 95 ml 2025-12-17 No No Current