FDA.reportPublic FDA data

Matte Velvet Tint

Product NDC
85334-203
11-digit product format
853340203
Labeler code
85334
Product ID
85334-203_45c8c79a-b4b6-d4be-e063-6394a90a9251
Type
HUMAN OTC DRUG
Nonproprietary name
Titanium Dioxide, Zinc Oxide
Dosage form
CREAM
Route
TOPICAL
Labeler
Brent Loftis, D.O., Inc., A California Medical Corporation
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-04-19
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
Matte Velvet Tint
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
85334-203-15Matte Velvet Tint1.5 g in 1 PACKETCREAM1.52
85334-203-50Matte Velvet Tint53 g in 1 BOTTLE, PUMPCREAM532

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
85334-203MATTE VELVET TINT (TITANIUM DIOXIDE, ZINC OXIDE) CREAM [BRENT LOFTIS, D.O., INC., A CALIFORNIA MEDICAL CORPORATION]1Current NDC, 1 package rows20250522_3583f860-664b-2658-e063-6394a90a3857.zip
85334-203MATTE VELVET TINT (TITANIUM DIOXIDE, ZINC OXIDE) CREAM [BRENT LOFTIS, D.O., INC., A CALIFORNIA MEDICAL CORPORATION]1Current NDC, 1 package rows20250522_359641c5-0e19-f243-e063-6394a90aeebc.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
85334-203-15853340203151.5 g in 1 PACKET (85334-203-15) 1.5 g2024-04-19YesNoCurrent
85334-203-508533402035053 g in 1 BOTTLE, PUMP (85334-203-50) 53 g2024-04-19NoNoCurrent