NATURAL SUN AQ SUPER WHITE SUN SPF50 PA

Dosage form: cream
Ingredients: TITANIUM DIOXIDE 1.36mL in 50mL
Labeler: THEFACESHOP CO., LTD.
NDC Code: 51523-022

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.

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.

NATURAL SUN AQ SUPER WHITE SUN  SPF50 PA
titanium dioxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51523-022
Route of AdministrationCUTANEOUSDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (TITANIUM) TITANIUM DIOXIDE1.36 mL  in 50 mL
Packaging
#Item CodePackage Description
1NDC:51523-022-0150 mL in 1 CARTON
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35204/01/2010
Labeler - THEFACESHOP CO., LTD. (688329416)

Revised: 07/2010
 
THEFACESHOP CO., LTD.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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