HUMCO CHARCOAL ACTIVATED- activated charcoal powder

Humco Charcoal Activated by

Drug Labeling and Warnings

Humco Charcoal Activated by is a Otc medication manufactured, distributed, or labeled by Humco Holding Group. Inc., Pharma Nobis, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

HUMCO CHARCOAL ACTIVATED 
activated charcoal powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0395-0527
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (ACTIVATED CHARCOAL - UNII:2P3VWU3H10)	ACTIVATED CHARCOAL	1000 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0395-0527-91	28 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/13/2017
2	NDC: 0395-0527-98	227 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/13/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		01/01/2008

Labeler - Humco Holding Group. Inc. (825672884)

Registrant - Humco Holding Group. Inc. (825672884)

Establishment
Name	Address	ID/FEI	Business Operations
Humco Holding Group, Inc.		825672884	analysis(0395-0527) , pack(0395-0527) , label(0395-0527) , manufacture(0395-0527)