Label: THE SKIN HOUSE ROSE HEAVENEMULSION- adenosine, niacinamide emulsion
- NDC Code(s): 73590-0049-1
- Packager: NOKSIBCHO cosmetic 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 April 8, 2020
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
Water
Carbomer
Butylene glycol
Cetyl Ethylhexanoate
Caprylic/Capric Triglyceride
Glycerin
Sodium Hyaluronate
Phenoxy ethanol
Glyceryl Stearate
PEG-100 Stearate
Glyceryl polyacrylate
1,2-Hexanediol
Cetyl Alcohol
Stearyl Alcohol
Myristyl Alcohol
Lauryl Alcohol
Sorbitan Stearate
Squalane
Rosa Canina Fruit Oil
Polysorbate 80
Butyrospermum Parkii (Shea Butter)
Tocopheryl Acetate
Dimethicone
Acanthopanax Senticosus (Eleuthero) Root Extract
Punica Granatum Fruit Extract
Carthamus Tinctorius (Safflower) Flower Extract
Propyliene glycol
Red ginseng extract
Rose Extract
Cyclomethicone
Arginine
Hyssopus Officinalis Extract
Myrciaria Dubia Fruit Extract
Malpighia Emarginata (Acerola) Fruit Extract
Paeonia Lactiflora Extract
Chrysanthemum Indicum Flower Extract
Leontopodium alpinum extract
Lonicera Japonica (Honeysuckle) Flower Extract
Lilium Tigrinum Extract
Malva Sylvestris (Mallow) Flower Extract
Thymus Vulgaris (Thyme) Extract
Xanthan GUM
Ethylhexylglycerin
Parfum - PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
-
WARNINGS
For external use only
When using this product■ if the following symptoms occurs after use, stop use and consult with a skin specialist
red specks, swelling, itching
■ don’t use on the part where there is injury, eczema, or dermatitis
Keep out of reach of children
■ if swallowed, get medical help or contact a person control center immediately
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
THE SKIN HOUSE ROSE HEAVENEMULSION
adenosine, niacinamide emulsionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73590-0049 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 WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73590-0049-1 130 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/08/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/08/2020 Labeler - NOKSIBCHO cosmetic Co., Ltd. (690182175) Registrant - NOKSIBCHO cosmetic Co., Ltd. (690182175) Establishment Name Address ID/FEI Business Operations NOKSIBCHO cosmetic Co., Ltd. 690182175 manufacture(73590-0049)