NATURAL SUN AQ SUPER WHITE SUN SPF50 PA- titanium dioxide cream

NATURAL SUN AQ SUPER WHITE SUN by

Drug Labeling and Warnings

NATURAL SUN AQ SUPER WHITE SUN by is a Otc medication manufactured, distributed, or labeled by THEFACESHOP CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient: TITANIUM DIOXIDE

INACTIVE INGREDIENT

Inactive Ingredients:

WATER, CYCLOPENTASILOXANE, ETHYLHEXYL METHOXYCINNAMATE, SD ALCOHOL 40-B, CYCLOMETHICONE, DICAPRYLYL CARBONATE, OCTYLDODECYL NEOPENTANOATE, SORBITAN STEARATE, SORBITYL LAURATE, DIPROPYLENE, GLYCOL, DIISOPROPYL ADIPATE, POTASSIUM CETYL PHOSPHATE, CETEARYL ALCOHOL, PEG-100 STEARATE,
GLYCERYL STEARATE DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, DIMETHICONE, METHYL METHACRYLATE CROSSPOLYMER, SILICA, METHICONE, RHEUM UNDULATUM ROOT/STALK/STEM EXTRACT, COPTIS CHINENSIS ROOT EXTRACT, GLYCERIN, ARGANIA SPINOSA KERNEL EXTRACT, CRAMBE MARITIMA EXTRACT, CAPRYLIC/CAPRIC TRIGLYCERIDE, MORUS ALBA BARK EXTRACT, GLYCYRRHIZA GLABRA (LICORICE) ROOT EXTRACT, ALOE FEROX LEAF EXTRACT, ETHYLHEXYL SALICYLATE, ARCTIUM LAPPA ROOT EXTRACT, ARTEMISIA PRINCEPS LEAF EXTRACT, POLYESTER-5, STEARIC ACID, XANTHAN GUM, PINUS STROBUS BARK EXTRACT, BUTYL METHOXYDIBENZOYLMETHANE, HYDROGENATED LECITHIN, POLYGLYCERYL-6 POLYRICINOLEATE, ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER, 4-METHYLBENZYLIDENE CAMPHOR, ISOAMYL P-METHOXYCINNAMATE, CAPRYLIC/CAPRIC GLYCERIDES, DISODIUM EDTA, METHYLPARABEN POTASSIUM HYDROXIDE, FRAGRANCE

DESCRIPTION

Warnings:
When using this product
Keep out of eyes. Rinse with water to remove.
Stop use and ask a doctor if
Rash or irritation develops and lasts.

Directions:
Apply evenly before sun exposure and as needed.
Children under 6months of age; ask a doctor.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NATURAL SUN AQ SUPER WHITE SUN  SPF50 PA
titanium dioxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51523-022
Route of Administration	CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM - UNII:D1JT611TNE)	TITANIUM DIOXIDE	1.36 mL  in 50 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51523-022-01	50 mL in 1 CARTON

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	04/01/2010

Labeler - THEFACESHOP CO., LTD. (688329416)