Home NDC 71220-087 Innisfree Daily UV Defense Mineral Sunscreen
Product NDC 71220-087
11-digit product format 712200087
Labeler code 71220
Product ID 71220-087_53c29cf3-b3ab-ff54-e063-6394a90a6f34
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide Lotion
Dosage form LOTION
Route TOPICAL
Labeler Innisfree Corporation
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-02-01
Substance ZINC OXIDE
Active strength 8 g/50mL
NDC exclude flag No
Listing certified through 2027-12-31
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 Innisfree Daily UV Defense Mineral Sunscreen
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 8 g/50mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SOI2LOH54Z Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71220-087-08 Innisfree Daily UV Defense Mineral Sunscreen 1 in 1 BOX LOTION 1 4 71220-087-08 Innisfree Daily UV Defense Mineral Sunscreen 50 mL in 1 TUBE LOTION 50 4 71220-087-41 Innisfree Daily UV Defense Mineral Sunscreen 10 mL in 1 TUBE LOTION 10 4 71220-087-41 Innisfree Daily UV Defense Mineral Sunscreen 1 in 1 BOX LOTION 1 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71220-087 INNISFREE DAILY UV DEFENSE MINERAL SUNSCREEN (ZINC OXIDE LOTION) LOTION [INNISFREE CORPORATION] 4 Current NDC, 4 package rows 20241105_0e9cd3e5-cff8-7594-e063-6394a90aad90.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 71220-087-08 71220008708 1 TUBE in 1 BOX (71220-087-08) / 50 mL in 1 TUBE 1 tube 2024-02-01 No No Current 71220-087-41 71220008741 1 TUBE in 1 BOX (71220-087-41) / 10 mL in 1 TUBE 1 tube 2024-07-01 No No Current