Home NDC 72085-307 SEA STAR SPARKLE SPF 50 Glitter Sunscreen Cotton Candy
Product NDC 72085-307
11-digit product format 720850307
Labeler code 72085
Product ID 72085-307_097478f1-9b4a-b749-e063-6394a90a9977
Type HUMAN OTC DRUG
Nonproprietary name HOMOSALATE, OCTOCRYLENE, OCTISALATE, ZINC OXIDE
Dosage form CREAM
Route TOPICAL
Labeler MJ Products Association, LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-08-10
Substance HOMOSALATE; OCTOCRYLENE; OCTISALATE; ZINC OXIDE
Active strength 100; 50; 50; 40 mg/mL; mg/mL; mg/mL; mg/mL
Pharmacologic classes Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
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 SEA STAR SPARKLE SPF 50 Glitter Sunscreen Cotton Candy
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 100 mg/mL OCTOCRYLENE 50 mg/mL OCTISALATE 50 mg/mL ZINC OXIDE 40 mg/mL
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 72085-307-05 SEA STAR SPARKLE SPF 50 Glitter Sunscreen Cotton Candy 5 mL in 1 PACKET CREAM 5 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72085-307 SEA STAR SPARKLE SPF 50 GLITTER SUNSCREEN COTTON CANDY (HOMOSALATE, OCTOCRYLENE, OCTISALATE, ZINC OXIDE) CREAM [MJ PRODUCTS ASSOCIATION, LLC] 3 Current NDC, Legacy NDC, 1 package rows 20231106_6ccd648f-ec3b-4325-8d89-b5dd10c2fff7.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 128 of 357 · 7,139 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 72085-307-05 72085030705 5 mL in 1 PACKET (72085-307-05) 5 ml 2020-08-10 0000-00-00 No No Current