Home NDC 50390-232 Artistry Youth Xtend Lifting Smoothing Foundation Shade Sand
Product NDC 50390-232
11-digit product format 503900232
Labeler code 50390
Product ID 50390-232_085b6df0-ddea-06ff-e063-6294a90abe0e
Type HUMAN OTC DRUG
Nonproprietary name OCTINOXATE, OXYBENZONE
Dosage form CREAM
Route TOPICAL
Labeler Amway Corp
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2013-05-06
Substance OCTINOXATE; OXYBENZONE
Active strength 75; 5 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 Artistry Youth Xtend Lifting Smoothing Foundation Shade Sand
Brand name suffix L2W1
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTINOXATE 75 mg/mL OXYBENZONE 5 mg/mL
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 95OOS7VE0Y 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 50390-232-00 Artistry Youth Xtend Lifting Smoothing Foundation Shade Sand L2W1 1 in 1 CARTON CREAM 1 2 50390-232-00 Artistry Youth Xtend Lifting Smoothing Foundation Shade Sand L2W1 30 mL in 1 BOTTLE, PLASTIC CREAM 30 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 50390-232 ARTISTRY YOUTH XTEND LIFTING SMOOTHING FOUNDATION SHADE SAND L2W1 (OCTINOXATE, OXYBENZONE) CREAM [AMWAY CORP] 2 Current NDC, Legacy NDC, 2 package rows 20231023_410592f1-57f5-4c17-8162-a0c088f0bf27.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 Marketing start Marketing end Sample Exclude flag Status 50390-232-00 50390023200 1 BOTTLE, PLASTIC in 1 CARTON (50390-232-00) / 30 mL in 1 BOTTLE, PLASTIC 2013-05-06 0000-00-00 No No Current