Home NDC 79487-150 Pure Sunscreen
Product NDC 79487-150
11-digit product format 794870150
Labeler code 79487
Product ID 79487-150_4eca5257-6844-2a33-e063-6394a90ade28
Type HUMAN OTC DRUG
Nonproprietary name AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Dosage form CREAM
Route TOPICAL
Labeler Liz Corporation Ltd
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-04-06
Substance OCTOCRYLENE; AVOBENZONE; OCTISALATE; HOMOSALATE
Active strength 3; 1.5; 2.25; 4 g/50g; g/50g; g/50g; g/50g
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 Pure Sunscreen
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTOCRYLENE 3 g/50g AVOBENZONE 1.5 g/50g OCTISALATE 2.25 g/50g HOMOSALATE 4 g/50g
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 79487-150-01 Pure Sunscreen 50 g in 1 TUBE CREAM 50 1 79487-150-02 Pure Sunscreen 1 in 1 BOX CREAM 1 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 302 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 79487-150-01 79487015001 50 g in 1 TUBE 50 g Historical 79487-150-02 79487015002 1 TUBE in 1 BOX (79487-150-02) / 50 g in 1 TUBE (79487-150-01) 1 tube 2026-04-06 No No Current