FDA.reportPublic FDA data

Daily Skin Protection Sunscreen Tinted

Product NDC
85479-208
11-digit product format
854790208
Labeler code
85479
Product ID
85479-208_46019888-02ad-317e-e063-6394a90a5f35
Type
HUMAN OTC DRUG
Nonproprietary name
Zinc Oxide
Dosage form
CREAM
Route
TOPICAL
Labeler
SKINPLUSBYOROYO LLC
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-04-21
Substance
ZINC OXIDE
Active strength
160 mg/g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Daily Skin Protection Sunscreen Tinted
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ZINC OXIDE160 mg/g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiSOI2LOH54Z

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85479-208-15Daily Skin Protection Sunscreen Tinted1.5 g in 1 PACKETCREAM1.52
85479-208-50Daily Skin Protection Sunscreen Tinted50 g in 1 BOTTLE, PUMPCREAM502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
85479-208DAILY SKIN PROTECTION SUNSCREEN TINTED (ZINC OXIDE) CREAM [SKINPLUSBYOROYO LLC]1Current NDC, 1 package rows20250523_35a9ecd7-b416-0aab-e063-6294a90a323d.zip
85479-208DAILY SKIN PROTECTION SUNSCREEN TINTED (ZINC OXIDE) CREAM [SKINPLUSBYOROYO LLC]1Current NDC, 1 package rows20250523_35aa194a-9a2e-2b5f-e063-6294a90a9877.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
85479-208-15854790208151.5 g in 1 PACKET (85479-208-15) 1.5 g2025-04-21YesNoHistorical
85479-208-508547902085050 g in 1 BOTTLE, PUMP (85479-208-50) 50 g2025-04-21NoNoHistorical