Label: NATURAL SUN AQ POWER LONG LASTING SUN SPF45 PA- zinc oxide cream
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Contains inactivated NDC Code(s)
NDC Code(s): 51523-020-01 - Packager: THEFACESHOP CO., LTD.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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 Label Information
Updated July 14, 2010
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- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive ingredients:
WATER, CYCLOPENTASILOXANE, BUTYLENE GLYCOL, ETHYLHEXYL METHOXYCINNAMATE, PEG-10 DIMETHICONE, DIPROPYLENE GLYCOL, DIMETHICONE, CETYL ETHYLHEXANOATE, MAGNESIUM SULFATE, QUATERNIUM-18 HECTORITE, DIMETHICONE CROSSPOLYMER, DIMETHICONE/PEG-10/15 CROSSPOLYMER, PANTHENOL, PONCIRUS TRIFOLIATA FRUIT EXTRACT, PORTULACA OLERACEA EXTRACT, SORBITAN SESQUIOLEATE, ZINC STEARATE, DIMETHICONE/METHICONE COPOLYMER, ALUMINUM HYDROXIDE, STEARIC ACID, METHYLPARABEN, FRAGRANCE, DISTEARYLDIMONIUM CHLORIDE, VP/EICOSENE COPOLYMER, MICA, ACRYLATES/DIMETHICONE COPOLYMER, NYLON-12, DIPOTASSIUM GLYCYRRHIZATE, ETHYLPARABEN, PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE, IRON OXIDES(CI 77492), VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER, IRON OXIDES(CI 77491), TOCOPHERYL ACETATE, METHICONE, IRON OXIDES(CI 77499), TRIETHOXYCAPRYLYLSILANE, CAPRYLIC/CAPRIC TRIGLYCERIDE, ALCOHOL, GLYCERIN, ARGANIA SPINOSA KERNEL EXTRACT, RHEUM UNDULATUM ROOT/STALK/STEM EXTRACT, SODIUM COCOYL GLUTAMATE, CARBOMER, COPTIS CHINENSIS ROOT EXTRACT, CRAMBE MARITIMA EXTRACT
- DESCRIPTION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
NATURAL SUN AQ POWER LONG LASTING SUN SPF45 PA
zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51523-020 Route of Administration CUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC OXIDE 5.5 mL in 50 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM - UNII:D1JT611TNE) TITANIUM DIOXIDE 2.25 mL in 50 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51523-020-01 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)