Home NDC 72043-2640 EltaMD UV Restore Tinted
Product NDC 72043-2640
11-digit product format 720432640
Labeler code 72043
Product ID 72043-2640_8e23ebeb-73f9-4ce6-b22b-6be66e04cc86
Type HUMAN OTC DRUG
Nonproprietary name titanium dioxide and zinc oxide sunscreen
Dosage form LOTION
Route TOPICAL
Labeler CP Skin Health Group, Inc.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-09-15
Marketing end 2028-08-31
Substance TITANIUM DIOXIDE; ZINC OXIDE
Active strength 20; 150 g/1000g; g/1000g
Pharmacologic classes Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
NDC exclude flag No
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 Restore Tinted Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM DIOXIDE 20 g/1000g ZINC OXIDE 150 g/1000g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 15FIX9V2JP Internal UNII lookup SOI2LOH54Z 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 72043-2640-1 EltaMD UV Restore Tinted 14 g in 1 BOTTLE LOTION 14 7 72043-2640-2 EltaMD UV Restore Tinted 57 g in 1 TUBE LOTION 57 7 72043-2640-3 EltaMD UV Restore Tinted 48 g in 1 BOTTLE LOTION 48 7 72043-2640-4 EltaMD UV Restore Tinted 2 g in 1 PACKET LOTION 2 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72043-2640 ELTAMD UV RESTORE TINTED (TITANIUM DIOXIDE AND ZINC OXIDE SUNSCREEN) LOTION [CP SKIN HEALTH GROUP, INC.] 6 Current NDC, Legacy NDC, 4 package rows 20240612_6a48ad0d-20e4-44b1-90d6-30bfbc68a152.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 81 of 354 · 7,077 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 72043-2640-1 72043264001 14 g in 1 BOTTLE (72043-2640-1) 14 g 2022-07-07 2028-08-31 No No Current 72043-2640-2 72043264002 57 g in 1 TUBE (72043-2640-2) 57 g 2020-09-15 0000-00-00 No No Current 72043-2640-3 72043264003 48 g in 1 BOTTLE (72043-2640-3) 48 g 2024-06-10 2027-07-31 No No Historical 72043-2640-4 72043264004 2 g in 1 PACKET (72043-2640-4) 2 g 2020-09-15 2028-03-31 No No Current