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Name:Natural Sun Aq Super White Sunspf50 Pa
Manufacturer:Thefaceshop Co., Ltd.
Category:Over-the-counter (OTC) Marketed Drugs


Drug Facts

NATURAL SUN AQ SUPER WHITE SUN SPF50 PA - titanium dioxide cream 
THEFACESHOP CO., LTD.

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 Ingredient: TITANIUM DIOXIDE

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

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.

Image of carton


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 DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TITANIUM DIOXIDE (TITANIUM) TITANIUM DIOXIDE 1.36 mL  in 50 mL
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:51523-022-01 50 mL in 1 CARTON None

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)

Revised: 07/2010 THEFACESHOP CO., LTD.



Source: http://dailymed.nlm.nih.gov
Reproduced with permission of U.S. National Library of Medicine


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