Home NDC 0096-0690 SOLBAR SUNSCREEN 35 AVO
Product NDC 0096-0690
11-digit product format 000960690
Labeler code 0096
Product ID 0096-0690_48f6bd1d-2d24-2a48-e063-6294a90abbcd
Type HUMAN OTC DRUG
Nonproprietary name Sunscreen
Dosage form CREAM
Route TOPICAL
Labeler Person and Covey
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-01-22
Substance HOMOSALATE; OCTINOXATE; AVOBENZONE; OXYBENZONE
Active strength 80; 75; 30; 60 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 SOLBAR SUNSCREEN 35 AVO
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 80 mg/g OCTINOXATE 75 mg/g AVOBENZONE 30 mg/g OXYBENZONE 60 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 Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0096-0690-03 SOLBAR SUNSCREEN 35 AVO 90 g in 1 TUBE CREAM 90 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 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 0096-0690-03 00096069003 90 g in 1 TUBE (0096-0690-03) 90 g 2026-01-22 No No Current