Innisfree Daily UV Defense Mineral Sunscreen

Product NDC
71220-087
11-digit product format
712200087
Labeler code
71220
Product ID
71220-087_2619fd9d-f9e1-18c1-e063-6394a90aa334
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
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Innisfree Daily UV Defense Mineral Sunscreen
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ZINC OXIDE8 g/50mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiSOI2LOH54Z

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71220-087-08Innisfree Daily UV Defense Mineral Sunscreen1 in 1 BOXLOTION14
71220-087-08Innisfree Daily UV Defense Mineral Sunscreen50 mL in 1 TUBELOTION504
71220-087-41Innisfree Daily UV Defense Mineral Sunscreen10 mL in 1 TUBELOTION104
71220-087-41Innisfree Daily UV Defense Mineral Sunscreen1 in 1 BOXLOTION14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71220-087INNISFREE DAILY UV DEFENSE MINERAL SUNSCREEN (ZINC OXIDE LOTION) LOTION [INNISFREE CORPORATION]4Current NDC, 4 package rows20241105_0e9cd3e5-cff8-7594-e063-6394a90aad90.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71220-087-08712200087081 TUBE in 1 BOX (71220-087-08) / 50 mL in 1 TUBE1 tube2024-02-01NoNoHistorical
71220-087-41712200087411 TUBE in 1 BOX (71220-087-41) / 10 mL in 1 TUBE1 tube2024-07-01NoNoHistorical