ING AMPOULE- glycerin, allantoin liquid

ING AMPOULE by

Drug Labeling and Warnings

ING AMPOULE by is a Otc medication manufactured, distributed, or labeled by DAONMEDICOS CO.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

GLYCERIN

INACTIVE INGREDIENT

Dipropylene Glycol, Pentylene Glycol, Saccharomyces/Artemisia Princeps Leaf Ferment Filtrate, Niacinamide, Sodium , Chondroitin Sulfate, Hexacarboxymethyl Dipeptide-12, rh-Oligopeptide-1(10ppm), Butylene Glycol, Water, Yeast Extract, Butylene Glycol, Water, Yeast Beta-Glucan, Butylene Glycol, Water, Morus Alba Leaf Extract, Water, ,
an Adipocyte Conditioned Media Extract, ytosphingosine, ramide NP, ospholipids, prylyl Glycol, opolone, ytosterols, ualane
1,2-Hexanediol, -Decapeptide-7 , -Octapeptide-4, -Oligopeptide-9, -Pentapeptide-19, galloyl Tetrapeptide-19 , ipeptide-48,
cotinoyl Tripeptide-1, lmitoyl Pentapeptide-4 , alicin, opanediol , ter, drolyzed Pea Protein , ytosterols, cithin , ea Europaea , live) Fruit Oil, sqalane, Butyrospermum Parkii (Shea) Butter, Ceramide NP, Butylene Glycol, Water, Centella Asiatica Extract ,
Polygonum Cuspidatum Root Extract, Scutellaria Baicalensis Root Extract, Camellia Sinensis Leaf Extract , Glycyrrhiza Glabra (Licorice) Root Extract , hamomilla Recutita (Matricaria) Flower Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract,
Butylene Glycol, Water, Triticum Vulgare (Wheat) Seed Extract , Butylene Glycol, Water, Echinacea Angustifolia Extract,
Glycerin, Water, Swiftlet Nest Extract, Butylene Glycol, Water, Pueraria Lobata Root Extract, Dimethicone, Water, Glycerin,
Butylene Glycol, PEG-20 Glyceryl Isostearate, Pentylene Glycol, Tocopheryl Acetate, Dimethicone/Vinyl Dimethicone, Crosspolymer, Diglycerin, 1,2-Hexanediol, Butylene Glycol, Copper Tripeptide-1 , Polysorbate 80, Propanediol , Aloe Barbadensis Leaf Extract, Bioflavonoids, Brassica Oleracea Italica (Broccoli) Extract, Sodium Polystyrene Sulfonate,
Dipotassium Glycyrrhizate, Cetyl Ethylhexanoate, Dimethyl Sulfone, Allantoin, Adenosine, Fragrance, Nonapeptide-29 ,Hexapeptide-8 , Nonapeptide-29 Pentapeptide-4, Panthenol, Isopentyldiol , Polyglyceryl-4 Oleate , Sucrose Palmitate
Ceramide NP, Propanediol , Butylene Glycol

PURPOSE

■ to reduce effectively the intensity of skin defects

■ skin looks lighter

■ reawakened for 7 days

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

spread evenly over the skin

WARNINGS

■ if following abnormal symptoms occurs after use , stop use and consult with a skin specialist

red specks, swelling, itching

■ don’t use on the part where there is injury, eczema, or dermatitis

Keep out of reach of children

■ if swallowed, get medical help or contact a person control center immediately

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ING AMPOULE 
glycerin, allantoin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72943-0001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	3 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALLANTOIN (UNII: 344S277G0Z)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72943-0001-1	90 mL in 1 BOX; Type 0: Not a Combination Product	03/24/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part347	03/24/2019

Labeler - DAONMEDICOS CO. (694819928)

Registrant - DAONMEDICOS CO. (694819928)

Establishment
Name	Address	ID/FEI	Business Operations
DAONMEDICOS CO.		694819928	manufacture(72943-0001) , label(72943-0001) , pack(72943-0001)