FDA.reportPublic FDA data

Proceuticals Private Label by TiZO Tinted Facial Mineral Sunscreen Backbar

Product NDC
58892-201
11-digit product format
588920201
Labeler code
58892
Product ID
58892-201_2be9f92a-a042-0595-e063-6394a90af7a8
Type
HUMAN OTC DRUG
Nonproprietary name
Titanium Dioxide, Zinc Oxide
Dosage form
CREAM
Route
TOPICAL
Labeler
Fallien Cosmeceuticals, LTD
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2014-03-01
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
Proceuticals Private Label by TiZO Tinted Facial Mineral Sunscreen Backbar
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
58892-201-85Proceuticals Private Label by TiZO Tinted Facial Mineral Sunscreen Backbar85 g in 1 BOTTLE, PUMPCREAM851

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58892-201PROCEUTICALS PRIVATE LABEL BY TIZO TINTED FACIAL MINERAL SUNSCREEN BACKBAR (TITANIUM DIOXIDE, ZINC OXIDE) CREAM [FALLIEN COSMECEUTICALS, LTD]1Current NDC, 1 package rows20250124_2be9f92a-a041-0595-e063-6394a90af7a8.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
58892-201-855889202018585 g in 1 BOTTLE, PUMP (58892-201-85) 85 g2014-03-01NoNoCurrent