FDA.reportPublic FDA data

Advanced Light Perfecting Sunscreen

Product NDC
85351-208
11-digit product format
853510208
Labeler code
85351
Product ID
85351-208_4586c8f3-33e8-111f-e063-6394a90ad8dd
Type
HUMAN OTC DRUG
Nonproprietary name
Zinc Oxide
Dosage form
CREAM
Route
TOPICAL
Labeler
ADVANCED DERMATOLOGY
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2021-09-01
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
Advanced Light Perfecting Sunscreen
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
85351-208-15Advanced Light Perfecting Sunscreen1.5 g in 1 PACKETCREAM1.52
85351-208-50Advanced Light Perfecting Sunscreen50 g in 1 BOTTLE, PUMPCREAM502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
85351-208ADVANCED LIGHT PERFECTING SUNSCREEN (ZINC OXIDE) CREAM [ADVANCED DERMATOLOGY]1Current NDC, 1 package rows20250417_32d781ca-7993-9875-e063-6294a90a5c26.zip
85351-208ADVANCED LIGHT PERFECTING SUNSCREEN (ZINC OXIDE) CREAM [ADVANCED DERMATOLOGY]1Current NDC, 1 package rows20250418_32e6c080-6ce3-8d99-e063-6294a90ac1bc.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
85351-208-15853510208151.5 g in 1 PACKET (85351-208-15) 1.5 g2021-09-01YesNoCurrent
85351-208-508535102085050 g in 1 BOTTLE, PUMP (85351-208-50) 50 g2021-09-01NoNoCurrent