Home NDC 49967-356 NYX Professional Makeup Buttermelt Glaze SOFT GLOW SKIN TINT SUNSCREEN BROAD SPECTRUM SPF 30
Product NDC 49967-356
11-digit product format 499670356
Labeler code 49967
Product ID 49967-356_ba362322-15b6-44a7-9eee-e80fe2c7c804
Type HUMAN OTC DRUG
Nonproprietary name Homosalate,Octisalate and Octocrylene
Dosage form CREAM
Route TOPICAL
Labeler L�Oreal USA Products Inc
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-01-10
Substance HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength 73; 50; 60 mg/mL; 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 NYX Professional Makeup Buttermelt Glaze SOFT GLOW SKIN TINT SUNSCREEN BROAD SPECTRUM SPF 30
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 73 mg/mL OCTISALATE 50 mg/mL OCTOCRYLENE 60 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination V06SV4M95S Internal UNII lookup 4X49Y0596W Internal UNII lookup 5A68WGF6WM Internal UNII lookup
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 49967-356-01 NYX Professional Makeup Buttermelt Glaze SOFT GLOW SKIN TINT SUNSCREEN BROAD SPECTRUM SPF 30 30 mL in 1 TUBE CREAM 30 2 49967-356-01 NYX Professional Makeup Buttermelt Glaze SOFT GLOW SKIN TINT SUNSCREEN BROAD SPECTRUM SPF 30 1 in 1 CARTON CREAM 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49967-356 NYX PROFESSIONAL MAKEUP BUTTERMELT GLAZE SOFT GLOW SKIN TINT SUNSCREEN BROAD SPECTRUM SPF 30 (HOMOSALATE,OCTISALATE AND OCTOCRYLENE) CREAM [L’OREAL USA PRODUCTS INC] 2 Current NDC, 2 package rows 20241225_81093d80-dcaf-4555-98b2-48ce7eb84d0c.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 Sample Exclude flag Status 49967-356-01 49967035601 1 TUBE in 1 CARTON (49967-356-01) / 30 mL in 1 TUBE 1 tube 2024-01-10 No No Current