Label: INTOMEDI FIRST AMPOULE PLACENTA- adenosine liquid
- NDC Code(s): 82879-0005-1, 82879-0005-2
- Packager: Janytree Inc.
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated July 12, 2022
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
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INACTIVE INGREDIENTS
Water, Hydrolyzed Horse Placenta Extract(150,000ppm), Ethyl Ascorbyl Ether, Dipropylene
Glycol, Lactobacillus/Hydrolyzed Pea Seed Extract Ferment Filtrate(Bio-Peptone®),
1,2-Hexanediol, Glycerin, Butylene Glycol, Dimethyl Sulfone, Centella Asiatica Extract,
Dexpanthenol, Pentylene Glycol, Mentha Piperita (Peppermint) Extract, Allantoin,
Sodium Hyaluronate, Hydrolyzed Collagen, Scutellaria Baicalensis Root Extract, Polygonum
Cuspidatum Root Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Portulaca Oleracea Extract,
Camellia Sinensis Leaf Extract, Sodium Hyaluronate Crosspolymer, Rosmarinus Officinalis
(Rosemary) Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract, Copper Tripeptide-1 - ACTIVE INGREDIENTS
- PURPOSE
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WARNINGS
For external use only When using this product
■ If following abnormal symptoms occurs after using the product, stop using the product and consult with a skin specialist. Symptoms : Red specks, swelling, itching
■ Do not use on the skin parts affected by wound, eczema, or dermatitis.
Keep out of reach of children.
■ If swallowed, get a medical help or contact a person in control center immediately.
■ Avoid contact with eyes. - KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
INTOMEDI FIRST AMPOULE PLACENTA
adenosine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82879-0005 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE 0.1 g in 100 mL Inactive Ingredients Ingredient Name Strength BUTYLENE GLYCOL (UNII: 3XUS85K0RA) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82879-0005-2 5 in 1 PACKAGE 07/13/2022 1 NDC:82879-0005-1 5 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/13/2022 Labeler - Janytree Inc. (688403840) Registrant - Janytree Inc. (688403840) Establishment Name Address ID/FEI Business Operations Janytree Inc. 688403840 manufacture(82879-0005)
