Home NDC 72043-6808 EltaMD UV SPF35
Product NDC 72043-6808
11-digit product format 720436808
Labeler code 72043
Product ID 72043-6808_b988dc70-eb19-4c6d-935e-74439188a438
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 2024-05-31
Substance ZINC OXIDE; OCTINOXATE
Active strength 70; 75 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 SPF35
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 70 g/1000g OCTINOXATE 75 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 4Y5P7MUD51 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 72043-6808-2 EltaMD UV SPF35 2 g in 1 PACKET LOTION 2 4 72043-6808-3 EltaMD UV SPF35 85 g in 1 TUBE LOTION 85 4 72043-6808-8 EltaMD UV SPF35 226 g in 1 TUBE LOTION 226 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72043-6808 ELTAMD UV SPF35 (OCTINOXATE, ZINC OXIDE SUNSCREEN) LOTION [CP SKIN HEALTH GROUP, INC] 2 Current NDC, 3 package rows 20240802_3029d6ed-a60b-4789-a567-d09b12d76bf4.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 45 of 354 · 7,077 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 72043-6808-2 72043680802 2 g in 1 PACKET (72043-6808-2) 2 g 2024-08-01 No No Current 72043-6808-3 72043680803 85 g in 1 TUBE (72043-6808-3) 85 g 2025-06-04 No No Current 72043-6808-8 72043680808 226 g in 1 TUBE (72043-6808-8) 226 g 2024-05-31 No No Current