Label: JUVEHEAL B AMPOULE- niacinamide, adenosine liquid
- NDC Code(s): 81689-020-01, 81689-020-02
- Packager: J MEDICAL Inter Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated June 21, 2021
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
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INACTIVE INGREDIENTS
Nelumbo Nucifera Flower Water, Butylene Glycol, Water, Glycerin, 1,2-Hexanediol, Camellia Sinensis Leaf Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Schisandra Chinensis Fruit Extract, Zingiber Officinale (Ginger) Root Extract, Asiaticoside, Betaine, Sodium Hyaluronate, Centella Asiatica Extract, Aloe Barbadensis Leaf Juice, Hydrolyzed Collagen, Sodium DNA, PEG-60 Hydrogenated Castor Oil, Allantoin, Beta-Glucan, Dipotassium Glycyrrhizate, Trehalose, Glutathione, sh-Oligopeptide-1, Caprylyl glycol, Ethylhexylglycerin, Fragrance
- PURPOSE
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WARNINGS
1. For external use only
2. Keep out of reach of children
3. If sympoms such as redness, swelling, itching or irritation occur by being exposed to direct sunlight during or after using cosmetics, consult a doctor.
4. Not to be applied over wound
5. Test the product by placing a small amount on the inside of your elbow and waiting 24 hours to see any skin reactions. - KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- Other information
- QUESTIONS
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
JUVEHEAL B AMPOULE
niacinamide, adenosine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81689-020 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 Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.04 g in 100 mL Inactive Ingredients Ingredient Name Strength NELUMBO NUCIFERA FLOWER OIL (UNII: P658Q19EG2) Butylene Glycol (UNII: 3XUS85K0RA) Water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81689-020-02 5 in 1 CARTON 03/01/2021 1 NDC:81689-020-01 5 mL in 1 CONTAINER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/01/2021 Labeler - J MEDICAL Inter Co., Ltd. (694065206) Registrant - J MEDICAL Inter Co., Ltd. (694065206) Establishment Name Address ID/FEI Business Operations J MEDICAL Inter Co., Ltd. 695439825 manufacture(81689-020)