Home NDC 72220-003 MDP UV BIO SUNSCREEN
Product NDC 72220-003
11-digit product format 722200003
Labeler code 72220
Product ID 72220-003_30877734-91d7-34c8-e063-6294a90a0e64
Type HUMAN OTC DRUG
Nonproprietary name ZINC OXIDE, HOMOSALATE, OCTOCRYLENE, OCTISALATE
Dosage form CREAM
Route TOPICAL
Labeler SKINIDEA CO., LTD
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-03-01
Substance ZINC OXIDE; HOMOSALATE; OCTOCRYLENE; OCTISALATE
Active strength 103.8; 60; 50; 45 mg/mL; mg/mL; mg/mL; mg/mL
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 MDP UV BIO SUNSCREEN
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 103.8 mg/mL HOMOSALATE 60 mg/mL OCTOCRYLENE 50 mg/mL OCTISALATE 45 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
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 72220-003-01 MDP UV BIO SUNSCREEN 40 mL in 1 TUBE CREAM 40 1 72220-003-02 MDP UV BIO SUNSCREEN 1 in 1 CARTON CREAM 1 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72220-003 MDP UV BIO SUNSCREEN (ZINC OXIDE, HOMOSALATE, OCTOCRYLENE, OCTISALATE) CREAM [SKINIDEA CO., LTD] 1 Current NDC, 2 package rows 20250319_3087771e-2ab8-2198-e063-6294a90a37d4.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 72220-003-01 72220000301 40 mL in 1 TUBE 40 ml Historical 72220-003-02 72220000302 1 TUBE in 1 CARTON (72220-003-02) / 40 mL in 1 TUBE (72220-003-01) 1 tube 2025-03-01 No No Current