Label: ING AMPOULE- glycerin, allantoin liquid
-
Contains inactivated NDC Code(s)
NDC Code(s): 72943-0001-1 - Packager: DAONMEDICOS CO.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 March 23, 2019
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
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
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
-
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
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
ING AMPOULE
glycerin, allantoin liquidProduct 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)
