Label: TENUE WHITENNING TONE UPCREAM- adenosine, niacinamide cream
- NDC Code(s): 82083-0013-1
- Packager: LAON COMMERCE co ltd
- Category: HUMAN OTC DRUG LABEL
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 October 26, 2022
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
Water
Butylene Glycol
Cyclopentasiloxane
Glycerin
Glycereth-26
Isoamyl Laurate
1,2-Hexanediol
Cetyl Ethylhexanoate
Caprylic/Capric Triglyceride
Niacinamide
Titanium Dioxide
Cyclohexasiloxane
Butylene Glycol Dicaprylate/Dicaprate
Polysorbate 60
Betaine
Prunus Amygdalus Dulcis (Sweet Almond) Oil
Butyrospermum Parkii (Shea Butter)
Polyacrylamide
Dimethiconol
Arginine
Carbomer
C13-14 Isoparaffin
Malpighia Emarginata (Acerola) Fruit Extract
Portulaca Oleracea Extract
Nelumbo Nucifera Flower Extract
Rosmarinus Officinalis (Rosemary) Leaf Extract
Chamomilla Recutita (Matricaria) Flower Extract
Olea Europaea (Olive) Fruit Extract
Melaleuca Alternifolia (Tea Tree) Extract
Tremella Fuciformis (Mushroom) Extract
Centella Asiatica Extract
Salvia Officinalis (Sage) Leaf Extract
Salix Alba (Willow) Bark Extract
Aluminum Hydroxide
Laureth-7
Allantoin
Adenosine
Disodium EDTA
Dipotassium Glycyrrhizate
Sodium Hyaluronate
Fragrance
Triethoxycaprylylsilane
Ethylhexylglycerin - PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
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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 WHITENNING TONE UPCREAM
adenosine, niacinamide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82083-0013 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 NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 2 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:82083-0013-1 50 mL in 1 TUBE; Type 0: Not a Combination Product 10/27/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/27/2022 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(82083-0013) , label(82083-0013)