Label: GOAT MILK AND LAVENDER SUN FOR BABY SPF 20 PA PLUS PLUS- octinoxate lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 76214-033-01 - Packager: SKINFOOD 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 October 4, 2011
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- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive ingredients:
WATER, PROPYLENE GLYCOL, ISOAMYL p-METHOXYCINNAMATE, BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE, CETEARYL ALCOHOL, CETYL ALCOHOL, HYDROXYETHYL UREA, LAVANDULA ANGUSTIFOLIA (LAVENDER) WATER, C14-22 ALCOHOLS, POLYSORBATE 80, GLYCERYL STEARATE, PEG-100 STEARATE, POLYGLYCERYL-3 METHYLGLUCOSE DISTEARATE, DIMETHICONE, SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER, C12-20 ALKYL GLUCOSIDE, ISOHEXADECANE, CHAMOMILLA RECUTITA (MATRICARIA) FLOWER EXTRACT, GOAT MILK EXTRACT, TOCOPHERYL ACETATE, CENTELLA ASIATICA EXTRACT, GLYCINE SOJA (SOYBEAN) SEED EXTRACT, GLYCYRRHIZA GLABRA (LICORICE) ROOT EXTRACT, DISODIUM EDTA, PHENOXYETHANOL, METHYLPARABEN, PROPYLPARABEN, FRAGRANCE
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
GOAT MILK AND LAVENDER SUN FOR BABY SPF 20 PA PLUS PLUS
octinoxate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76214-033 Route of Administration CUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 4.9 mL in 70 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 3.15 mL in 70 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CETYL ALCOHOL (UNII: 936JST6JCN) HYDROXYETHYL UREA (UNII: MBQ7DDQ7AR) LAVANDULA ANGUSTIFOLIA FLOWERING TOP (UNII: 9YT4B71U8P) C14-22 ALCOHOLS (UNII: B1K89384RJ) POLYSORBATE 80 (UNII: 6OZP39ZG8H) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) PEG-100 STEARATE (UNII: YD01N1999R) DIMETHICONE (UNII: 92RU3N3Y1O) PHENOXYETHANOL (UNII: HIE492ZZ3T) C12-20 ALKYL GLUCOSIDE (UNII: K67N5Z1RUA) METHYLPARABEN (UNII: A2I8C7HI9T) ISOHEXADECANE (UNII: 918X1OUF1E) CHAMOMILE (UNII: FGL3685T2X) GOAT MILK (UNII: XE5K5I4RP7) PROPYLPARABEN (UNII: Z8IX2SC1OH) CENTELLA ASIATICA (UNII: 7M867G6T1U) SOYBEAN (UNII: L7HT8F1ZOD) GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) EDETATE DISODIUM (UNII: 7FLD91C86K) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76214-033-01 70 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 03/01/2011 Labeler - SKINFOOD CO., LTD. (690324173) Registrant - SKINFOOD CO., LTD. (690324173) Establishment Name Address ID/FEI Business Operations SKINFOOD CO., LTD. 690324173 manufacture