Label: OBEO 7WAY MOISTURE- glycerin lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 69871-003-01, 69871-003-02 - Packager: CPbio 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 January 25, 2016
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
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INACTIVE INGREDIENT
Water, Xanthan Gum, Disodium EDTA, Butylene Glycol, Triethanolamine, Hydrogenated C6-14 Olefin Polymers, Caprylic/Capric Triglyceride, Polysorbate 60, Butyrospermum Parkii (Shea) Butter, Hydrogenated Lecithin, Stearic acid, Sorbitan Stearate, Glyceryl Stearate, PEG-100 Stearate, Cetearyl Alcohol, Carbomer, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Isohexadecane, Polysorbate 80, Caprylhydroxamic Acid, 1,2-Hexanediol, Caprylyl Glycol, Boswellia Serrata Resin Extract, Fragrance, Mineral Water, Sodium Hyaluronate, Propandiol, Saccharomyces/Viscum Album (Mistletoe) Ferment Extract, Saccharomyces/Imperata Cylindrica Root Ferment Extract, Lactobacillus/Soybean Ferment Extract, Human Oligopeptide-1, Caprylyl Glycol, Oryza Sativa (Rice) Callus Culture Extract
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
OBEO 7WAY MOISTURE
glycerin lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69871-003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 16 mg in 200 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) XANTHAN GUM (UNII: TTV12P4NEE) EDETATE DISODIUM (UNII: 7FLD91C86K) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) TROLAMINE (UNII: 9O3K93S3TK) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) POLYSORBATE 60 (UNII: CAL22UVI4M) SHEA BUTTER (UNII: K49155WL9Y) HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N) STEARIC ACID (UNII: 4ELV7Z65AP) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) PEG-100 STEARATE (UNII: YD01N1999R) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC) SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX) ISOHEXADECANE (UNII: 918X1OUF1E) POLYSORBATE 80 (UNII: 6OZP39ZG8H) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) CAPRYLYL GLYCOL (UNII: 00YIU5438U) INDIAN FRANKINCENSE (UNII: 4PW41QCO2M) HYALURONATE SODIUM (UNII: YSE9PPT4TH) PROPANEDIOL (UNII: 5965N8W85T) VISCUM ALBUM FRUITING TOP (UNII: BK9092J5MP) IMPERATA CYLINDRICA ROOT (UNII: VYT2JA85NH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69871-003-02 1 in 1 CARTON 01/25/2016 1 NDC:69871-003-01 200 mL in 1 CONTAINER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/25/2016 Labeler - CPbio Co., Ltd (689514410) Registrant - CPbio Co., Ltd (689514410) Establishment Name Address ID/FEI Business Operations CPbio Co., Ltd 689514410 manufacture(69871-003)