Label: HUMCO CHARCOAL ACTIVATED- activated charcoal powder

  • NDC Code(s): 0395-0527-91, 0395-0527-98
  • Packager: Humco Holding Group. Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 15, 2023

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

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Charcoal Activated

  • Purpose

    First Aid Poison Adsorbent

  • OTHER SAFETY INFORMATION

    If possibl;e, call a Poison Control Center, emergency facility, or health professional for help before using this product. If help cannot be reached quickly, follow the directions in this label. Read the warnings and directions as soon as you buy this product. Insert emergency phone number(s) in space proviedd on the label.

    Poison Control Center: 1-800-222-1222

    Emergency Medical Facility: ____________________

    Health Professional: _____________________

  • Warning:

    Do not use if Tamper Evident Seal imprinted "Sealed for Your Protection" is broken or missing. This product is sealed with either a shrink band around the cap or foil seal under cap.

  • Use

    For emergency use to adsorb swallowed poisons.

  • Warnings

    • Do not give Activated Charcoal until after patient has vomited unless directed by a health professional.
    • Do not use in persons who are not fully conscious.
    • Do not use this product unless directed by a health professional if turpentine, corrosives such as alkalies (lye) and strong acids or petroleum didtillates, such as kerosene, gasoline, paint thinner, cleaning fluid or furniture polish have been ingested.
    • Do not give if poison victim is unconscious or having convulsions. Keep patient active and moving.
  • Keep out of reach of children.

    In case of accidental overdose, seek professional assistance or contact a Poison Control Center immediately.

  • Directions for 1 oz bottle

    When Activated Charcoal is indicated for use, give 3 to 4 heaping tablespoonfulls (20 to 30 g) mixed in a minimum of 8 ounces of liquid or as directed by a health professional. If an emergency, fill this bottle with water.

    Mix well and have poison victim drink all of this mixture. Repeat dose immediately, if possible. If previous attempts to contact a poison control center, emergency medical center or health professional were unsuccessful, continue trying. If possible save the container of poison.

  • Directions for 8 oz bottle

    When Activated Charcoal is indicated, the usual dose is as follows:

    • 0-10 years of age: 1 to 3 heaping tablespoonfulls (10 -25 g) mixed in a minimum of 8 ounces of liquid.
    • 10 - 12 yrs of age: 3 - 6 tablespoonfulls (25 - 50 g) mixed in a minimum of 8 ounces of liquid.
    • Greater than 12 years of age: 3 to 12 tablespoonfulls (25 - 100g) mixed with a minimum of 8 ounces of liquid or as directed by a health professional. mix well and have poison victim drink all of this mixture. Repeat dose immediately, if possible. If the previous attempts to contact poison control center, emergency medical center or health professional were unsuccessful, continue trying. If possible save the container of poison.
  • Other Information

    • Activated Charcoal has a very gritty texture and will coat the mouth, lips and tonge.
    • Keep tightly closed in a cool dry place.
  • Inactive Ingredients

    None

  • Principal Display Panel

    capture

  • INGREDIENTS AND APPEARANCE
    HUMCO CHARCOAL ACTIVATED 
    activated charcoal powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0395-0527
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (ACTIVATED CHARCOAL - UNII:2P3VWU3H10) ACTIVATED CHARCOAL1000 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0395-0527-9128 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/13/2017
    2NDC:0395-0527-98227 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/13/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02301/01/2008
    Labeler - Humco Holding Group. Inc. (825672884)
    Registrant - Pharma Nobis, LLC (118564114)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pharma Nobis, LLC118564114analysis(0395-0527) , pack(0395-0527) , label(0395-0527) , manufacture(0395-0527)