Mineral Sunscreen Tinted

Product NDC
85558-203
11-digit product format
855580203
Labeler code
85558
Product ID
85558-203_46285af9-d7d6-9794-e063-6394a90a8d00
Type
HUMAN OTC DRUG
Nonproprietary name
Titanium Dioxide, Zinc Oxide
Dosage form
CREAM
Route
TOPICAL
Labeler
LOTUS SKINCARE AND MAKE-UP STUDIO
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2022-10-28
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
Mineral Sunscreen Tinted
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
85558-203-50Mineral Sunscreen Tinted53 g in 1 BOTTLE, PUMPCREAM532

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
85558-203-508555802035053 g in 1 BOTTLE, PUMP (85558-203-50) 53 g2022-10-28NoNoCurrent