Home NDC 72043-2522 EltaMD UV AOX Elements
Product NDC 72043-2522
11-digit product format 720432522
Labeler code 72043
Product ID 72043-2522_df80438e-9164-4f29-941f-fcdfbcbc2e63
Type HUMAN OTC DRUG
Nonproprietary name zinc oxide, titanium dioxide sunscreen
Dosage form LOTION
Route TOPICAL
Labeler CP Skin Health Group, Inc
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-05-01
Substance ZINC OXIDE; TITANIUM DIOXIDE
Active strength 135.1; 44.3 g/1000g; g/1000g
Pharmacologic classes Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
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 EltaMD UV AOX Elements
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 135.1 g/1000g TITANIUM DIOXIDE 44.3 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.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72043-2522-1 EltaMD UV AOX Elements 48 g in 1 BOTTLE LOTION 48 1 72043-2522-2 EltaMD UV AOX Elements 2 g in 1 PACKET LOTION 2 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72043-2522 ELTAMD UV AOX ELEMENTS (ZINC OXIDE, TITANIUM DIOXIDE SUNSCREEN) LOTION [CP SKIN HEALTH GROUP, INC] 1 Current NDC, 2 package rows 20250503_d01756c0-1f82-4e08-b956-8000ecaddfd1.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 Units Marketing start Sample Exclude flag Status 72043-2522-1 72043252201 48 g in 1 BOTTLE (72043-2522-1) 48 g 2025-05-01 No No Current 72043-2522-2 72043252202 2 g in 1 PACKET (72043-2522-2) 2 g 2025-05-01 No No Current