NATURAL SUN AQ SUPER PERFECT SUN SPF50 PA

Dosage form: cream
Ingredients: TITANIUM DIOXIDE 1.36mL in 50mL
Labeler: THEFACESHOP CO., LTD.
NDC Code: 51523-021

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, CYCLOMETHICONE, DIPROPYLENE GLYCOL, ETHYLHEXYL METHOXYCINNAMATE, GLYCERIN, CETEARYL ALCOHOL, OCTYLDODECYL NEOPENTANOATE, DICAPRYLYL CARBONATE, POTASSIUM CETYL PHOSPHATE, TRICETEARETH-4 PHOSPHATE, GLYCOL STEARATE, PEG-2 STEARATE, POLYETHYLENE, GLYCERYL STEARATE, PEG-100 STEARATE, STEARIC ACID, POLYGLYCERYL-6 POLYRICINOLEATE, RHEUM UNDULATUM ROOT/STALK/STEM EXTRACT, COPTIS CHINENSIS ROOT EXTRACT, XANTHAN GUM, POLYESTER-5, CAPRYLIC/CAPRIC GLYCERIDES, CAPRYLIC/CAPRIC TRIGLYCERIDE, CRAMBE MARITIMA EXTRACT, CARAPA GUAIANENSIS SEED OIL, ARGANIA SPINOSA KERNEL EXTRACT, HYDROGENATED LECITHIN, SILICA, METHICONE, ACRYLATES/ACRYLAMIDE COPOLYMER, MINERAL OIL, POLYSORBATE 85, ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER, TRIETHANOLAMINE, METHYLPARABEN, DISODIUM EDTA, ETHYLHEXYL SALICYLATE, ISOAMYL-p METHOXYCINNAMATE, 4-METHYLBENZYLIDENE CAMPHOR, BUTYL METHOXYDIBENZOYLMETHANE, FRAGRANCE, ALPHA-ISOMETHYL IONONE, BENTYL BENZOATE, BUTYLPHENY METHYLPROPIONAL, CITRONELLOL, HEXYL CINNAMAL,  LIMONENE, LINALOOL

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 PERFECT SUN  SPF50 PA
titanium dioxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51523-021
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:51523-021-0150 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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