Label: CHARMZONE ALBATROSS POWDER SUN (SPF41 PA)- octinoxate octisalate zinc oxide titanium dioxide cream
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Contains inactivated NDC Code(s)
NDC Code(s): 22201-2001-1 - Packager: CHARMZONE 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 November 9, 2009
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ACTIVE INGREDIENT
Label2
INGREDIENTS:
WATER, ETHYLHEXYL METHOXYCINNAMATE, BUTYLENE GLYCOL, POLYMETHYL METHACRYLATE, ETHYLHEXYL DIMETHYL PABA, ETHYLHEXYL SALICYLATE, HYDROGENATED POLYDECENE, ZINC OXIDE, SILICA, CYCLOMETHICONE, BUTYL METHOXYDIBENZOYLMETHANE, BIOSACCHARIDE GUM-1, TITANIUM DIOXIDE, BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE, CETYL ALCOHOL, CETEARETH-12, GLYCERYL STEARATE, PEG-100 STEARATE, SODIUM HYALURONATE, STEARIC ACID, DIETHOXYETHYL SUCCINATE, GLYCERYL POLYACRYLATE, SORBITAN OLIVATE, BEESWAX, CETEARYL OLIVATE, CETYL PALMITATE, AMMONIUM ACRYLOYLDIMETHYLTAURATE / VP COPOLYMER, PHENOXYETHANOL, SORBITAN PALMITATE, TOCOPHERYL ACETATE, POTASSIUM CETYL PHOSPHATE, METHYLPARABEN, TRIETHOXYCAPRYLYLSILANE, FRAGRANCE, BIFIDA FERMENT LYSATE, BUTYLPARABEN, DIPOTASSIUM GLYCYRRHIZATE, HYDROLYZED SOY PROTEIN, MORUS ALBA ROOT EXTRACT, PEG-1182 METHYL ESTER SERICIN, PROPYLPARABEN, XANTHAN GUM, MAGNESIUM ASCORBYL PHOSPHATE, BHT, DIMETHICON, FOMES OFFICINALIS (MUSHROOM) EXTRACT, DISODIUM EDTA, STEARYL GLYCYRRHETINATE, GLYCOSAMINOGLYCANS, ATELOCOLLAGEN, BAMBUSA ARUNDINACEA STEM EXTRACT, RUBUS SUAVISSIMUS (RASPBERRY) LEAF EXTRACT, PORTULACA OLEACEA EXTRACT, ANGELICA POLYMORPHA SINENSIS ROOT EXTRACT, ASPALATHUS LINEARIS LEAF EXTRACT, VISCUM ALBUM (MISTLETOE) LEAF EXTRACT
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INGREDIENTS AND APPEARANCE
CHARMZONE ALBATROSS POWDER SUN (SPF41 PA)
octinoxate octisalate zinc oxide titanium dioxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:22201-2001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 4.91 mL in 70 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 3.15 mL in 70 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC - UNII:J41CSQ7QDS) ZINC OXIDE 2.33 mL in 70 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM - UNII:D1JT611TNE) TITANIUM DIOXIDE 1.225 mL in 70 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:22201-2001-1 70 mL in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 12/01/2009 Labeler - CHARMZONE CO LTD (689049765) Registrant - CHARMZONE CO LTD (689049765) Establishment Name Address ID/FEI Business Operations CHARMZONE CO LTD 689049765 manufacture