Label: MU LAB TURN AROUND 2W REFRESH EX- niacinamide, adenosine cream
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Contains inactivated NDC Code(s)
NDC Code(s): 71164-020-01, 71164-020-02 - Packager: MU-Biz.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 December 30, 2016
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive Ingredients: WATER, CETYL ALCOHOL, GLYCERYL STEARATE, PEG-75 STEARATE, CETETH-20, STEARETH-20, SODIUM ASCORBYL PHOSPHATE, DIMETHYL SULFONE, 1,2-HEXANEDIOL, BUTYLENE GLYCOL, CAPRYLHYDROXAMIC ACID, POTASSIUM HYDROXIDE, CETEARYL ALCOHOL, SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL, SALICYLIC ACID, AZELAIC ACID, TOCOPHERYL ACETATE, CAPRYLIC/CAPRIC TRIGLYCERIDE, LAVANDULA ANGUSTIFOLIA (LAVENDER) OIL, GLYCERIN, OLIGOPEPTIDE-1, COPPER TRIPEPTIDE-1, ETHYLHEXYLGLYCERIN, HOUTTUYNIA CORDATA EXTRACT, GLYCYRRHIZA GLABRA (LICORICE) ROOT EXTRACT, LACTIC ACID, GLYCOLIC ACID
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- Use
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Directions
Directions: - Clean the skin thoroughly before using - Day and night, apply amount of one pumping onto forehead and nose, and massage in the order of forehead, nose->cheeks->eyes. The active ingredients are highly concentrated and need to be controlled in this way. The first area to come in contact with this product will be the most effected. So, for instance, apply the designated amount first around the eyes may irritate. Massage lightly. If no irritation is visible, increase amount through a 3-to-4-day interval.
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MU LAB TURN AROUND 2W REFRESH EX
niacinamide, adenosine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71164-020 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 0.40 g in 20 mL ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE 0.008 g in 20 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CETYL ALCOHOL (UNII: 936JST6JCN) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71164-020-02 1 in 1 CARTON 12/01/2016 1 NDC:71164-020-01 20 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/01/2016 Labeler - MU-Biz.co,.Ltd (689852174) Registrant - MU-Biz.co,.Ltd (689852174) Establishment Name Address ID/FEI Business Operations MU-Biz.co,.Ltd 689852174 relabel(71164-020) Establishment Name Address ID/FEI Business Operations B&B KOREA CO LTD 688499349 manufacture(71164-020)
