Label: AC ALL- glycerin liquid

  • Category: HUMAN OTC DRUG LABEL

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 October 17, 2014

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  • ACTIVE INGREDIENT

    glycerin


  • INACTIVE INGREDIENT

    blueberry ext, assai ext, indian gooseberry fruit ext, cranberry fruit ext, melon ext, rhus tree bark ext, lactobacillus, colloidal silver, lavender oil, etc


  • PURPOSE

    skin protection
    excellent antimicrobial
    safe for human body


  • KEEP OUT OF REACH OF CHILDREN

    keep out or reach of the children


  • INDICATIONS & USAGE

    1. Put 1-2 drops of AC ALL spot care ampule liquid on cotton bud or a vessel.
    2. Place watery cotton bud on the skin and gently push for 5 minutes until absorbed.
    3. Repeat 1 and 2 for 2-3 times, and 2 times a day.
    4. When suppuration has occurred as a secondary infection, remove it before use.
    5. Put a cotton swab dipped into the ampule lightly on the reddened spot for 5 seconds.
    6. Use lotions after the liquid is fully absorbed on skin.
    7. Trouble spots will disappear in 2-3 days, and generally skin will be improved in 1-2
    months.
    8. Use repetitively on troubled skin (Red or black marks) until the skin condition became
    better.(Do not reuse the cotton bud due to the risk of bacterial infection.)


  • WARNINGS

    - avoid direct sun exposure, keep it refrigerated or in cooler places
    - do not eat

  • DOSAGE & ADMINISTRATION

    for exernal use only


  • PRINCIPAL DISPLAY PANEL

    package label
  • INGREDIENTS AND APPEARANCE
    AC ALL 
    glycerin liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69224-2001
    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)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69224-2001-130 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34710/17/2014
    Labeler - GL BioTech (689057539)
    Registrant - GL BioTech (689057539)
    Establishment
    NameAddressID/FEIBusiness Operations
    GL BioTech 689057539manufacture(69224-2001)
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