Home NDC 72043-2601 EltaMD UV Active
Product NDC 72043-2601
11-digit product format 720432601
Labeler code 72043
Product ID 72043-2601_ebce3d40-92cb-40d4-a60f-917c51c3be92
Type HUMAN OTC DRUG
Nonproprietary name zinc oxide and titanium dioxide sunscreen
Dosage form CREAM
Route TOPICAL
Labeler CP Skin Health Group, Inc
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-08-03
Substance ZINC OXIDE; TITANIUM DIOXIDE
Active strength 190.1; 40.3 g/1000g; g/1000g
Pharmacologic classes Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
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 EltaMD UV Active
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 190.1 g/1000g TITANIUM DIOXIDE 40.3 g/1000g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SOI2LOH54Z Internal UNII lookup 15FIX9V2JP 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 Sample Exclude flag Status 72043-2601-3 72043260103 85 g in 1 TUBE (72043-2601-3) 85 g 2026-08-03 No No Current