Label: MEFACTORY 3STEP PIGGY NOSE PORE STRIP STEP 01 PORE OPENING SHEET- adenosine patch
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Contains inactivated NDC Code(s)
NDC Code(s): 70908-080-01 - Packager: MeFactory Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated March 3, 2017
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive ingredients: Purified water,Butylene Glycol,Glycerin,Trehalose ,Propanediol,Tremella Fuciformis (Mushroom) Extract,Glycolic Acid ,PEG-75 ,Citrus Grandis (Grapefruit) Seed Extract ,Acorus Calamus Root Extract,Perilla Ocymoides Leaf Extract ,Arginine,Hydrolyzed Collagen ,PEG-60 Hydrogenated Castor Oil ,Xanthan Gum ,Chlorphenesin ,Gaultheria Procumbens (Wintergreen) Leaf Extract,Adenosine ,Wine Extract ,Camellia Sinensis Leaf Extract ,Betula Platyphylla Japonica Juice ,Sea Water,Bambusa Vulgaris Water,Jasminum Officinale (Jasmine) Flower Water ,Rosa Damascena Flower Water ,Vanillyl Butyl Ether,1,2-Hexanediol ,Disodium EDTA ,Fragrance,Lactic Acid ,Betaine Salicylate
- PURPOSE
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WARNINGS
Warnings: 1. Discontinue use immediately and consult a dermatologist, if you experience the following: 1) Irritation, Red spots, itchy skin or rash 2) Applied skin area has the above reaction from direct sun 2. Do not use on irritated skin, cuts, or other infected skin area. 3. Avoid contact with eyes.
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MEFACTORY 3STEP PIGGY NOSE PORE STRIP STEP 01 PORE OPENING SHEET
adenosine patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70908-080 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.6 mg in 3 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Butylene Glycol (UNII: 3XUS85K0RA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70908-080-01 3 g in 1 POUCH; Type 0: Not a Combination Product 02/01/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 02/01/2017 Labeler - MeFactory Co., Ltd. (689840967) Registrant - MeFactory Co., Ltd. (689840967) Establishment Name Address ID/FEI Business Operations MeFactory Co., Ltd. 689840967 manufacture(70908-080)
