Ultra Protection Sunscreen

Product NDC
85563-202
11-digit product format
855630202
Labeler code
85563
Product ID
85563-202_4604168d-87eb-d709-e063-6394a90a79d5
Type
HUMAN OTC DRUG
Nonproprietary name
Titanium Dioxide, Zinc Oxide
Dosage form
CREAM
Route
TOPICAL
Labeler
CLEAR SKIN SOLUTIONS, LLC
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2021-06-10
Substance
TITANIUM DIOXIDE; ZINC OXIDE
Active strength
80; 38 mg/g; 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
Ultra Protection Sunscreen
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
TITANIUM DIOXIDE80 mg/g
ZINC OXIDE38 mg/g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii15FIX9V2JP, SOI2LOH54Z

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85563-202-50Ultra Protection Sunscreen53 g in 1 BOTTLE, PUMPCREAM532

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
85563-202ULTRA PROTECTION SUNSCREEN (TITANIUM DIOXIDE, ZINC OXIDE) CREAM [CLEAR SKIN SOLUTIONS, LLC]1Current NDC, 1 package rows20250523_35bc4586-5e62-c9e7-e063-6294a90a276b.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
85563-202-508556302025053 g in 1 BOTTLE, PUMP (85563-202-50) 53 g2021-06-10NoNoCurrent