Charcoal Activated

Manufacturer
Woodward Pharma Services LLC
Effective date
2018-06-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:54:32

Label at a glance#

ProductCharcoal Activated
Active ingredientACTIVATED CHARCOAL
Label structure11 sections

Dosage and administration

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 profe...

Label contents#

Full prescribing information#

OTHER SAFETY INFORMATION

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

OTC - ACTIVE INGREDIENT SECTION

Charcoal Activated

Purpose

OTC - PURPOSE SECTION

First Aid Poison Adsorbent

Use

INDICATIONS & USAGE SECTION

For emergency use to adsorb swallowed poisons.

Warnings

WARNINGS SECTION

  • Do not use 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 distillates, such as kerosene, gasoline, paint thinner, cleaning fluid or furniture polish have been ingested.
  • Do not use if poison victim is unconscious or having convulsions. Keep patient active and moving.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

OTHER SAFETY INFORMATION

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

Questions or comments?

OTC - QUESTIONS SECTION

Please call 888-514-4727

Inactive Ingredients

INACTIVE INGREDIENT SECTION

None

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1 oz label

Label 1 ozLabel 1 oz

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69784-308-282025-09-17C16284748780-1f386c649-e05e-0266-e053-dadaa90a7c1aCharcoal Activated
69784-308-282023-01-30C16284748780-1f386c649-e05e-0266-e053-dadaa90a7c1aCharcoal Activated

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69784-308CHARCOAL ACTIVATED POWDER [WOODWARD PHARMA SERVICES LLC]1Legacy NDC20180618_b0854d7b-24bc-4d65-bf59-6716b5f999b5.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
69784-308-28GM - Gram69784-308ef7a309c-db0b-4c47-ad75-64e044810d2312018-12-13

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69784-30869784-308-28

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ACTIVATED CHARCOAL2P3VWU3H10ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
8b19f3e8-5b30-4f77-9484-3544dadfad18b0854d7b-24bc-4d65-bf59-6716b5f999b52025-09-17WarningsExact identifier
spl set id: b0854d7b-24bc-4d65-bf59-6716b5f999b5

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.