GOAT MILK AND LAVENDER SUN FOR BABY SPF 20 PA PLUS PLUS- octinoxate lotion

GOAT MILK AND LAVENDER SUN by

Drug Labeling and Warnings

GOAT MILK AND LAVENDER SUN by is a Otc medication manufactured, distributed, or labeled by SKINFOOD CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients: OCTINOXATE 7%, OCTISALATE 4.5%

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

Purpose: Protects skin from UV rays.

WARNINGS

Warnings:
For external use only.
Avoid contact with eyes.
Discontinue use if signs of irritation appear.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children:
Keep out of reach of children.

INDICATIONS & USAGE

Indication and usage:
Use at the end of your daily skincare regimen.
Apply liberally onto face and body before sun exposure avoiding the eye area.

DOSAGE & ADMINISTRATION

Dosage and administration:
For best results, apply at least 15 to 20 minutes before sun exposure.
Reapply frequently while out in the sun.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GOAT MILK AND LAVENDER SUN  FOR BABY SPF 20 PA PLUS PLUS
octinoxate lotion

Product 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