Home NDC 72043-2920 UV Daily Deep Tint
Product NDC 72043-2920
11-digit product format 720432920
Labeler code 72043
Product ID 72043-2920_79386a40-776e-47d1-8909-88776673d1a9
Type HUMAN OTC DRUG
Nonproprietary name octinoxate, zinc oxide sunscreen
Dosage form LOTION
Route TOPICAL
Labeler CP Skin Health Group, Inc.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-05-09
Substance OCTINOXATE; ZINC OXIDE
Active strength 750; 900 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 UV Daily Deep Tint
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTINOXATE 750 g/1000g ZINC OXIDE 900 g/1000g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4Y5P7MUD51 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 72043-2920-1 UV Daily Deep Tint 50 g in 1 BOTTLE LOTION 50 1 72043-2920-2 UV Daily Deep Tint 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 72043-2920 UV DAILY DEEP TINT (OCTINOXATE, ZINC OXIDE SUNSCREEN) LOTION [CP SKIN HEALTH GROUP, INC.] 1 Current NDC, 2 package rows 20240511_c12fa9a4-d7e5-46bf-9bfb-1cbbaa73b450.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 72043-2920-1 72043292001 50 g in 1 BOTTLE (72043-2920-1) 50 g 2024-05-09 No No Current 72043-2920-2 72043292002 2 g in 1 PACKET (72043-2920-2) 2 g 2024-05-09 No No Current