Home NDC 87204-248 LUXE COLOR FOUNDATION
Product NDC 87204-248
11-digit product format 872040248
Labeler code 87204
Product ID 87204-248_576c3496-7030-808c-e063-6394a90a53c3
Type HUMAN OTC DRUG
Nonproprietary name Octinoxate 7% Zinc Oxide 5%
Dosage form EMULSION
Route TOPICAL
Labeler Guangzhou Huixue Biotechnology Co., Ltd.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-07-15
Marketing end 2027-07-20
Substance OCTINOXATE; ZINC OXIDE
Active strength .07; .05 mg/30mL; mg/30mL
NDC exclude flag No
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 LUXE COLOR FOUNDATION Active Ingredients# Ingredient, Strength table Ingredient Strength OCTINOXATE .07 mg/30mL ZINC OXIDE .05 mg/30mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4Y5P7MUD51 Internal UNII lookup SOI2LOH54Z Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 87204-248-01 87204024801 30 mL in 1 BOX, UNIT-DOSE (87204-248-01) 30 ml 2026-07-15 2027-07-20 No No Historical