Drug Facts

MOISTURIZING SUNBLOCK - titanium dioxide lotion
Vienna Health and Beauty Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active Ingredients:                      Purpose

Titanium Dioxide 8%                   Sunscreen
Octyl Methoxycinnamate 6%   Sunscreen
Benzophenone 3%                        Sunscreen

Other Ingredients: Purified Water (Acqua), Capryic/Capic Triglyceride, C12-15 Alkyl Benzoate, Glycerin, Cetyl Alcohol, Stearyl Alcohol, Isopropyl Myristate, Propylene Glycol, Ceteareth-6,Ceteareth-25, Dimethocone, Glyceryl Stearate, Stearic Acid, Tocopherol Acetate9Vitamin E), Alpha Bisabolol, Triethanolamine, Diazolidinyl Urea, Methylparaben, Propylparaben, Allantoin, BHT.

Vienna Health and Beauty - MOISTURIZING SUNBLOCK - UVA/UVB Protection - SPF30 image of carton

MOISTURIZING SUNBLOCK
titanium dioxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:52625-100
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	8 g in 100 g
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	6 g in 100 g
BENZOPHENONE (UNII: 701M4TTV9O) (BENZOPHENONE - UNII:701M4TTV9O)	BENZOPHENONE	3 g in 100 g

#	Item Code	Package Description
Packaging
1	NDC:52625-100-02	1 in 1 CARTON
1	NDC:52625-100-01	100 g in 1 JAR

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part352	07/01/2010

Labeler - Vienna Health and Beauty Corporation (831463919)

Registrant - Vienna Health and Beauty Corporation (831463919)

Name	Address	ID/FEI	Business Operations
Establishment
Vienna Health and Beauty Corporation		831463919	manufacture