Label: INTOMEDI FIRST AMPOULE CYSTEINE- niacinamide liquid
- NDC Code(s): 82879-0004-1, 82879-0004-2
- Packager: Janytree Inc.
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated July 12, 2022
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
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INACTIVE INGREDIENTS
Water, Ethyl Ascorbyl Ether, Dipropylene Glycol, Glycerin, 1,2-Hexanediol, Arbutin, Lactobacillus/
Hydrolyzed Pea Seed Extract Ferment Filtrate(Bio-Peptone®), Dimethyl Sulfone, Butylene
Glycol, Tranexamic Acid, Panthenol, Centella Asiatica Extract, Pentylene Glycol, Mentha Piperita
(Peppermint) Extract, Allantoin, Glutathione, Sodium Hyaluronate, Hydrolyzed Collagen, Scutellaria
Baicalensis Root Extract, Polygonum Cuspidatum Root Extract, Camellia Sinensis Leaf Extract,
Glycyrrhiza Glabra (Licorice) Root Extract, Sodium Hyaluronate Crosspolymer, Chamomilla Recutita
(Matricaria) Flower Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Acetyl Cysteine(50ppm) - 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 CYSTEINE
niacinamide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82879-0004 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 2 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:82879-0004-2 5 in 1 PACKAGE 07/13/2022 1 NDC:82879-0004-1 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(82879-0004)
