Label: JUVEHEAL A AMPOULE- adenosine liquid
- NDC Code(s): 81689-040-01, 81689-040-02
- Packager: J MEDICAL Inter Co., Ltd.
- 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 June 21, 2021
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENTS
Nelumbo Nucifera Flower Water, Water, Butylene Glycol, 1,2-Hexanediol, Bis-PEG-18 Methyl Ether Dimethyl Silane, Centella Asiatica Extract, Polygonum Cuspidatum Root Extract, Scutellaria Baicalensis Root Extract, Camellia Sinensis Leaf Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Chamomilla Recutita (Matricaria) Flower Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Sodium Hyaluronate, Allantoin, Hydrolyzed Collagen, Aloe Barbadensis Leaf Juice, Vincetoxicum Atratum Extract, Hydrolyzed Pea Protein, Phytosterols, Lecithin, Olea Europaea (Olive) Fruit Oil, Squalane, Butyrospermum Parkii (Shea) Butter, Ceramide NP (=Ceramide 3), PEG-60 Hydrogenated Castor Oil, Beta-Glucan, Dipotassium Glycyrrhizate, Glycerin, Glutathione, sh-Oligopeptide-1, sh-Polypeptide-1, Caprylyl Glycol, Chlorphenesin, Ethylhexylglycerin, Propanediol, 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 A AMPOULE
adenosine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81689-040 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.04 g in 100 mL Inactive Ingredients Ingredient Name Strength NELUMBO NUCIFERA FLOWER OIL (UNII: P658Q19EG2) Water (UNII: 059QF0KO0R) Butylene Glycol (UNII: 3XUS85K0RA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81689-040-02 5 in 1 CARTON 03/01/2021 1 NDC:81689-040-01 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(81689-040)
