Home NDC 68577-032 Ulta Beauty Tinted Moisturizer Cream Spf 24 Light
Product NDC 68577-032
11-digit product format 685770032
Labeler code 68577
Product ID 68577-032_2a269211-00ef-cfd4-e063-6394a90aab3a
Type HUMAN OTC DRUG
Nonproprietary name AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Dosage form CREAM
Route TOPICAL
Labeler Cosmax Usa, Corporation
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-06-01
Substance AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength 30; 95; 45; 50 mg/mL; 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 Ulta Beauty Tinted Moisturizer Cream Spf 24 Light
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 30 mg/mL HOMOSALATE 95 mg/mL OCTISALATE 45 mg/mL OCTOCRYLENE 50 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
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 68577-032-00 Ulta Beauty Tinted Moisturizer Cream Spf 24 Light 35 mL in 1 TUBE CREAM 35 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68577-032 ULTA BEAUTY TINTED MOISTURIZER CREAM SPF 24 LIGHT (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) CREAM [COSMAX USA, CORPORATION] 5 Current NDC, 1 package rows 20241228_fbbff4eb-a63e-b083-e053-6294a90a404a.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 241 of 352 · 7,030 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 68577-032-00 68577003200 35 mL in 1 TUBE (68577-032-00) 35 ml 2021-06-01 No No Current