Label: TENUE 24K GOLD AMPOULE- adenosine liquid
- NDC Code(s): 82083-0012-1
- Packager: LAON COMMERCE 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 September 18, 2022
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
Water
Glycerin
Butylene Glycol
Dipropylene Glycol
Betaine
1,2-Hexanediol
Trehalose
PEG-60 Hydrogenated Castor Oil
Sodium Hyaluronate
Salix Alba (Willow) Bark Extract
Melaleuca Alternifolia (Tea Tree) Extract
Olea Europaea (Olive) Fruit Extract
Nelumbo Nucifera Flower Extract
Portulaca Oleracea Extract
Tremella Fuciformis (Mushroom) Extract
Salvia Officinalis (Sage) Leaf Extract
Centella Asiatica Extract
Chamomilla Recutita (Matricaria) Flower Extract
Rosmarinus Officinalis (Rosemary) Leaf Extract
PVM/MA Copolymer
Carbomer
Triethanolamine
Allantoin
Camellia Sinensis Leaf Extract
Phenoxyethanol
Ethylhexylglycerin
Xanthan Gum
Disodium EDTA
Glyceryl Acrylate/Acrylic Acid Copolymer
Fragrance
Gold
CI 19140
CI 15985 - PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
-
WARNINGS
1. consult a specialist if there are any abnormal symptoms or side effects such as red spots, swelling, or itching due to direct sunlight when using cosmetics
2. avoid using them in areas with wounds
3. precautions for storage and handling
a) keep out of reach of childrea
b) keep away from direct sunlight
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
TENUE 24K GOLD AMPOULE
adenosine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82083-0012 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 WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82083-0012-1 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 09/19/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 09/19/2022 Labeler - LAON COMMERCE co ltd (557839830) Registrant - LAON COMMERCE co ltd (557839830) Establishment Name Address ID/FEI Business Operations LAON COMMERCE CO Ltd 557839830 manufacture(82083-0012) , label(82083-0012)