Home NDC 82046-692 La Roche Posay Anthelios Sunscreen SPF 60 Ultra light
Product NDC 82046-692
11-digit product format 820460692
Labeler code 82046
Product ID 82046-692_b53a13e6-4730-4d15-8991-482725bbbca0
Type HUMAN OTC DRUG
Nonproprietary name AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE
Dosage form SPRAY
Route TOPICAL
Labeler L'Oreal USA, Inc.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2014-01-01
Substance AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Active strength 27; 96; 29; 54; 35 mg/g; 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 La Roche Posay Anthelios Sunscreen SPF 60 Ultra light
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 27 mg/g HOMOSALATE 96 mg/g OCTISALATE 29 mg/g OCTOCRYLENE 54 mg/g OXYBENZONE 35 mg/g
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 Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 82046-692-01 La Roche Posay Anthelios Sunscreen SPF 60 Ultra light 143 g in 1 CAN SPRAY 143 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 82046-692 LA ROCHE POSAY ANTHELIOS SUNSCREEN SPF 60 ULTRA LIGHT (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [L'OREAL USA, INC.] 2 Current NDC, Legacy NDC, 1 package rows 20231222_dad00eee-92cd-7610-e053-2a95a90a1fac.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 26 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 82046-692-01 82046069201 143 g in 1 CAN (82046-692-01) 143 g 2014-01-01 0000-00-00 No No Current