Label: BODYHOLIC YELLOW POTION HAIR AND BODY MIST- glycerin spray

  • 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 April 13, 2017

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    Active ingredients: Glycerin 1.0%

  • INACTIVE INGREDIENT

    Inactive ingredients: Water, PEG-40 Hydrogenated Castor Oil, Alcohol, Fragrance, Phenoxyethanol, Erythritol, Butyl Methoxydibenzoylmethane, Disodium EDTA, Sodium Citrate, Citric Acid, Butylene Glycol, Centella Asiatica Extract, Polygonum Cuspidatum Root Extract, Scutellaria Baicalensis Root Extract, Camellia Sinensis Leaf Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Chamomilla Recutita (Matricaria) Flower Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Onsen-Sui

  • PURPOSE

    Purpose: Skin moisturizing

  • WARNINGS

    Warnings: For external use only Avoid contact with eyes. Discontinue use if signs of irritation or rashes appear. Replace the cap after use.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

  • Uses

    Uses: Spray on any area of your skin and hair except face to hydrate.

  • Directions

    Directions: Spray on any area of your skin and hair except face to hydrate.

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of carton

  • INGREDIENTS AND APPEARANCE
    BODYHOLIC YELLOW POTION HAIR AND BODY MIST 
    glycerin spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70908-130
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Glycerin (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) Glycerin0.5 g  in 50 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Alcohol (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70908-130-021 in 1 CARTON04/01/2017
    1NDC:70908-130-0150 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other04/01/2017
    Labeler - MeFactory Co., Ltd. (689840967)
    Registrant - MeFactory Co., Ltd. (689840967)
    Establishment
    NameAddressID/FEIBusiness Operations
    MeFactory Co., Ltd.689840967manufacture(70908-130)