Label: CAMELIA BODY- glycerin lotion

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated March 8, 2015

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

  • ACTIVE INGREDIENT

    glycerine


  • INACTIVE INGREDIENT

    water, lavender flower water, camellia seed oil, grape seed oil, jojoba seed oil, shea butter, olive fruit oil, castor seed oil, etc


  • PURPOSE

    skin protectant


  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

    towel dry your body completely after shower or bath
    put an appropriate amount of body lotion onto the palm of your hand and massage lotion gently to the skin


  • WARNINGS

    ・Stop using the product when you have skin problems or the product disagrees with your skin
    ・Stop using the product immediately and consult a dermatologist if you have redness, swelling, itching or irritation on the skin while or after using the product.
    ・Don't place the product in any place where it will be subjected to extremely high or low temperatures or direct sunlight.


  • DOSAGE & ADMINISTRATION

    for external use only

  • PRINCIPAL DISPLAY PANEL

    package label
  • INGREDIENTS AND APPEARANCE
    CAMELIA BODY 
    glycerin lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69602-1001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN2 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    DEXPANTHENOL (UNII: 1O6C93RI7Z)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69602-1001-1250 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34703/08/2015
    Labeler - Saebyuck Corp. (688427008)
    Registrant - Saebyuck Corp. (688427008)
    Establishment
    NameAddressID/FEIBusiness Operations
    Saebyuck Corp.688427008manufacture(69602-1001)