Home NDC 68577-253 ANEW ULTIMATE DAY MULTI-PERFORMANCECREAM SPF 25 SUNSCREEN
Product NDC 68577-253
11-digit product format 685770253
Labeler code 68577
Product ID 68577-253_562053f4-75d6-a8b1-e063-6394a90a01a8
Type HUMAN OTC DRUG
Nonproprietary name AVOBENZONE, HOMOSALATE, OCTINOXATE,OXYBENZONE
Dosage form CREAM
Route TOPICAL
Labeler COSMAX USA, CORPORATION
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-01-03
Substance OCTINOXATE; HOMOSALATE; OXYBENZONE; AVOBENZONE
Active strength 5; 8; 4; 2.85 g/100mL; g/100mL; g/100mL; g/100mL
NDC exclude flag No
Listing certified through 2027-12-31
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 ANEW ULTIMATE DAY MULTI-PERFORMANCECREAM SPF 25 SUNSCREEN
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTINOXATE 5 g/100mL HOMOSALATE 8 g/100mL OXYBENZONE 4 g/100mL AVOBENZONE 2.85 g/100mL
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.
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 81 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 68577-253-00 68577025300 1 JAR in 1 CARTON (68577-253-00) / 50 mL in 1 JAR 1 jar 2024-01-03 No No Current