Mineral Fusion Tinted

Product NDC
85416-203
11-digit product format
854160203
Labeler code
85416
Product ID
85416-203_457632ec-dde4-ba16-e063-6394a90a192a
Type
HUMAN OTC DRUG
Nonproprietary name
Titanium Dioxide, Zinc Oxide
Dosage form
CREAM
Route
TOPICAL
Labeler
FOREFRONT DERMATOLOGY, S.C.
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2021-02-04
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 Fusion 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
85416-203-15Mineral Fusion Tinted15 g in 1 PACKETCREAM152
85416-203-50Mineral Fusion Tinted53 g in 1 BOTTLE, PUMPCREAM532

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
85416-203MINERAL FUSION TINTED (TITANIUM DIOXIDE, ZINC OXIDE) CREAM [FOREFRONT DERMATOLOGY, S.C.]1Current NDC, 1 package rows20250423_334ec844-5560-50f7-e063-6394a90a01be.zip
85416-203MINERAL FUSION TINTED (TITANIUM DIOXIDE, ZINC OXIDE) CREAM [FOREFRONT DERMATOLOGY, S.C.]1Current NDC, 1 package rows20250423_334f90d6-68e5-db37-e063-6294a90a5fb1.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
85416-203-158541602031515 g in 1 PACKET (85416-203-15) 15 g2021-02-04YesNoCurrent
85416-203-508541602035053 g in 1 BOTTLE, PUMP (85416-203-50) 53 g2021-02-04NoNoCurrent