Home NDC 49967-906 Dermablend Professional Leg and Body Makeup Broad Spectrum SPF 25 Sunscreen
Product NDC 49967-906
11-digit product format 499670906
Labeler code 49967
Product ID 49967-906_234c562a-5b25-44b4-9ace-7c1021bf8cf3
Type HUMAN OTC DRUG
Nonproprietary name Octisalate and Octocrylene
Dosage form LOTION
Route TOPICAL
Labeler L'Oreal USA Products Inc
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2017-01-01
Substance OCTISALATE; OCTOCRYLENE
Active strength 32; 60 mg/mL; mg/mL
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 Dermablend Professional Leg and Body Makeup Broad Spectrum SPF 25 Sunscreen
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTISALATE 32 mg/mL OCTOCRYLENE 60 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4X49Y0596W Internal UNII lookup 5A68WGF6WM Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 49967-906-01 Dermablend Professional Leg and Body Makeup Broad Spectrum SPF 25 Sunscreen 100 mL in 1 TUBE LOTION 100 10 49967-906-01 Dermablend Professional Leg and Body Makeup Broad Spectrum SPF 25 Sunscreen 1 in 1 CARTON LOTION 1 10
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49967-906 DERMABLEND PROFESSIONAL LEG AND BODY MAKEUP BROAD SPECTRUM SPF 25 SUNSCREEN (OCTISALATE AND OCTOCRYLENE) LOTION [L'OREAL USA PRODUCTS INC] 10 Current NDC, Legacy NDC, 2 package rows 20241230_df62e1c2-ce72-4ded-8985-156dce9ff41d.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 49967-906-01 49967090601 1 TUBE in 1 CARTON (49967-906-01) / 100 mL in 1 TUBE 1 tube 2017-01-01 0000-00-00 No No Current