NATURALTH GOAT MILK MOISTURE- glycerin emulsion

NATURALTH GOAT MILK MOISTURE by

Drug Labeling and Warnings

NATURALTH GOAT MILK MOISTURE by is a Otc medication manufactured, distributed, or labeled by TONYMOLY CO.,LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient: Glycerin 6.00%

INACTIVE INGREDIENT

Inactive Ingredient: Water,Goat Milk Extract,Hydrogenated Polydecene,Butylene Glycol,CetylEthylhexanoate,1,2-Hexanediol,Polysorbate60, ButyrospermumParkii(Shea)Butter, GlycerylStearate,Panthenol,Cetearyl Alcohol,Polyglyceryl-3Methylglucose Distearate,BiosaccharideGum-1,Phenoxyethanol,SorbitanStearate, Dimethicone,PalmiticAcid,Carbomer, PEG-100 Stearate, Stearic Acid, Tromethamine, Polyacrylate-13,Polyisobutene, Ethylhexylglycerin,XanthanGum, Fragrance, Disodium EDTA, Polysorbate 20,Pantolactone,SorbitanIsostearate, Lecithin, Alcohol, Polysorbate 80, Sodium AscorbylPhosphate,Ceramide3, Anthocyanins,CitricAcid,Hydrolyzed Hyaluronic Acid

PURPOSE

Purpose: Skin Protectant

WARNINGS

Warnings: For external use only. When using this product do not get into eyes. Stop use and ask a doctor if rash occurs. Do not use on - deep puncture wounds - animal bites - serious burns Keep out of reach of children.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

Use

Use: Moisturizing seaweed lotion that supplies moisture to rough and dry skin

Directions

Directions: - clean the skin thoroughly before using - apply in daily skin care routine

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NATURALTH GOAT MILK MOISTURE 
glycerin emulsion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59078-280
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Glycerin (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	Glycerin	9 g  in 150 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Butylene Glycol (UNII: 3XUS85K0RA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59078-280-02	1 in 1 CARTON	05/01/2016
1	NDC: 59078-280-01	150 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/01/2016

Labeler - TONYMOLY CO.,LTD (688216798)

Registrant - TONYMOLY CO.,LTD (688216798)

Establishment
Name	Address	ID/FEI	Business Operations
TONYMOLY CO.,LTD		688216798	manufacture(59078-280)