CHARCOAL ACTIVATED- charcoal activated powder 
Woodward Pharma Services LLC

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.

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Charcoal Activated

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

Poison Control Center: 1-800-222-1222

Emergency Medical Facility: ____________________

Health Professional: _____________________

Active Ingredient

Charcoal Activated

Purpose

First Aid Poison Adsorbent

Use

For emergency use to adsorb swallowed poisons.

Warnings

Keep out of reach of children.

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

Directions

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.

Other Information

Questions or comments?

Please call 888-514-4727

Inactive Ingredients

None

Principal Display Panel

1 oz label

Label 1 oz

CHARCOAL ACTIVATED 
charcoal activated powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69784-308
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:69784-308-2828 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/01/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other06/01/2018
Labeler - Woodward Pharma Services LLC (026749066)
Registrant - Woodward Pharma Services LLC (026749066)

Revised: 6/2018
Document Id: 4a6309ee-4fe4-4b34-99e5-ef9bdcfa18a9
Set id: b0854d7b-24bc-4d65-bf59-6716b5f999b5
Version: 1
Effective Time: 20180601
 
Woodward Pharma Services LLC