Label: BRIGHTUNING PEPTIDE AMPOULE- niacinamide liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 73330-0002-1 - Packager: COSNINE, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated December 23, 2019
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Saccharomyces/Rice Ferment Filtrate
1,2-Hexanediol
Glyceryl Glucoside
Ananas Sativus (Pineapple) Fruit Extract
Butylene Glycol
Glycerin
Betaine
Disodium EDTA
Glyceryl Glucoside
Water
Glycerin
Methylpropanediol
Ammonium Acryloyldimethyltaurate/VP
Copolymer
Ammonium
Acryloyldimethyltaurate/Beheneth-25 Methacrylate Crosspolymer
Xanthan Gum
Polyglyceryl-6 Stearate
Polyglyceryl-6 Behenate
Caprylic/Capric Triglyceride
Polyglyceryl-3 Distearate
Glyceryl Stearate Citrate
Ethylhexylglycerin
Caprylyl Glycol
Ethylhexyl Palmitate
Glyceryl Stearate
Water
Butylene Glycol
1,2-Hexanediol
Sodium Hyaluronate
Glycerin
Water
Akebia Quinata Extract
1,2-Hexanediol
Water
Pentylene Glycol
Madecassoside
Melia Azadirachta Flower Extract
Ocimum Sanctum Leaf Extract
Melia Azadirachta Leaf Extract
Curcuma Longa (Turmeric) Root Extract
Corallina Officinalis Extract
Water
Eclipta Prostrata Extract
Water
Water
1,2-Hexanediol
Heptasodium Hexacarboxymethyl
Dipeptide-12
Water
1,2-Hexanediol
Pentasodium Tetracarboxymethyl
Acetylhydroxyprolyl Dipeptide-12
Pentasodium Tetracarboxymethyl
Dipeptide-51
Water
1,2-Hexanediol
Dipeptide-1 - PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
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WARNINGS
1. Do not use in the following cases(Eczema and scalp wounds)
2.Side Effects
1)Due to the use of this druf if rash, irritation, itching and symptopms of hypersnesitivity occur dicontinue use and consult your phamacisr or doctor
3.General Precautions
1)If in contact with the eyes, wash out thoroughty with water If the symptoms are servere, seek medical advice immediately
2)This product is for exeternal use only. Do not use for internal use
4.Storage and handling precautions
1)If possible, avoid direct sunlight and store in cool and area of low humidity
2)In order to maintain the quality of the product and avoid misuse
3)Avoid placing the product near fire and store out in reach of children - DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BRIGHTUNING PEPTIDE AMPOULE
niacinamide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73330-0002 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 WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73330-0002-1 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/15/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/06/2019 Labeler - COSNINE, Inc. (694607163) Registrant - COSNINE, Inc. (694607163) Establishment Name Address ID/FEI Business Operations COSNINE, Inc. 694607163 manufacture(73330-0002)