EZ Char

Manufacturer
Padagis US LLC
Effective date
2021-12-06
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 21:26:58

Label at a glance#

ProductEZ Char
Active ingredientACTIVATED CHARCOAL
Label structure10 sections

Dosage and administration

Remove Seal. Reconstitute into an oral suspension by adding 4 oz. of water to bottle, replacing cap and shaking well, or by pouring contents into a separate container, adding 4 oz. water, and stirring thoroughly. USE IMMEDIATELY, DO NOT STORE RECONSTITUTED PRODUCT. 6 to 12 lb 1 to 2 TBS of reconstituted liquid 12 to 24 lb 2 to 4 TBS of reconstituted liquid 24 to 48 lb 4 to 8 TBS of reconstituted liquid 48 lb + ent...

Storage and handling

• each bottle contains: magnesium 35 mg, potassium 18 mg, sodium 57 mg • if previous attempts to contact a poison control center, emergency medical facility, or health professional were unsuccessful, continue trying • keep patient active and moving • save the container of poison • store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature]

Label contents#

Full prescribing information#

Active ingredient (in each bottle)

OTC - ACTIVE INGREDIENT SECTION

Activated charcoal 25 grams

Purpose

OTC - PURPOSE SECTION

Poison adsorbent

Use

INDICATIONS & USAGE SECTION

for emergency use to adsorb swallowed poisons

Warnings

WARNINGS SECTION

  • do not give activated charcoal until after the patient has vomited unless directed by health professional
  • do not use in persons who are not fully conscious
  • do not use this product, unless directed by 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
  • TAMPER EVIDENT: DO NOT USE IF PROTECTIVE SEAL IS BROKEN OR MISSING

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Remove Seal. Reconstitute into an oral suspension by adding 4 oz. of water to bottle, replacing cap and shaking well, or by pouring contents into a separate container, adding 4 oz. water, and stirring thoroughly.

USE IMMEDIATELY, DO NOT STORE RECONSTITUTED PRODUCT.

6 to 12 lb

1 to 2 TBS of reconstituted liquid

12 to 24 lb

2 to 4 TBS of reconstituted liquid

24 to 48 lb

4 to 8 TBS of reconstituted liquid

48 lb +

entire amount of reconstituted liquid

Repeat dose immediately, if necessary.

Other information

STORAGE AND HANDLING SECTION

  • each bottle contains: magnesium 35 mg, potassium 18 mg, sodium 57 mg
  • if previous attempts to contact a poison control center, emergency medical facility, or health professional were unsuccessful, continue trying
  • keep patient active and moving
  • save the container of poison
  • store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature]

Inactive ingredient

INACTIVE INGREDIENT SECTION

bentonite

Questions?

OTC - QUESTIONS SECTION

1-800-328-5113 Serious side effects associated with use of this product may be reported to this number.

Package/Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

EZ Char®

ACTIVATED CHARCOAL PELLETS

POISON ADSORBENT

Read label warnings and directions upon buying this product. For help using this product call a Poison Control Center, emergency medical facility, or health professional. If help cannot be reached quickly, follow the directions on the label. In case of poisoning call your Poison Control Center at 1-800-222-1222.

NET WEIGHT 0.88 oz (25 grams)

label-rev05-19
label-rev05-19

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0574-0122EZ CHAR (ACTIVATED CHARCOAL) PELLET [PADAGIS US LLC]5Legacy NDC20230825_ff6811b0-d845-4d77-8edd-aaaa3d62ce99.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0574-0122-25EA - Each0574-01225536cce9-f674-4fe3-bf14-4b4f7b94d59012014-10-03

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ACTIVATED CHARCOALACTIVE INGREDIENT2P3VWU3H101
ACTIVATED CHARCOALACTIVE MOIETY2P3VWU3H101
BENTONITEINACTIVE INGREDIENTA3N5ZCN45C1

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
0574-01220574-0122-25

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
ACTIVATED CHARCOAL2P3VWU3H10ACTIB
BENTONITEA3N5ZCN45CIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 11 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
BENTONITEBENTONITEA3N5ZCN45CSHAMPOO, SUSPENSION / TOPICAL3.25 %w/vExact identifier — unii candidate
11 equally ranked IID candidates
BENTONITEBENTONITEA3N5ZCN45CPOWDER / TOPICAL0.67 mg/mgExact identifier — unii candidate
11 equally ranked IID candidates
BENTONITEBENTONITEA3N5ZCN45CTABLET, COATED / ORAL1.8 mgExact identifier — unii candidate
11 equally ranked IID candidates
BENTONITEBENTONITEA3N5ZCN45CLOTION / TOPICAL5 %w/wExact identifier — unii candidate
11 equally ranked IID candidates
BENTONITEBENTONITEA3N5ZCN45CCREAM / TOPICAL4.1 %w/wExact identifier — unii candidate
11 equally ranked IID candidates
BENTONITEBENTONITEA3N5ZCN45CSYSTEM / TRANSDERMAL9.86 mgExact identifier — unii candidate
11 equally ranked IID candidates
BENTONITEBENTONITEA3N5ZCN45CPOWDER, DENTIFRICE / DENTAL0.05 mg/mgExact identifier — unii candidate
11 equally ranked IID candidates
BENTONITEBENTONITEA3N5ZCN45CTABLET / ORAL355 mgExact identifier — unii candidate
11 equally ranked IID candidates
BENTONITEBENTONITEA3N5ZCN45CCAPSULE / ORALADJ PHExact identifier — unii candidate
11 equally ranked IID candidates
BENTONITEBENTONITEA3N5ZCN45CSUPPOSITORY / VAGINAL288.1 mgExact identifier — unii candidate
11 equally ranked IID candidates
BENTONITEBENTONITEA3N5ZCN45CSUSPENSION / ORAL65 mg/5mlExact identifier — unii candidate
11 equally ranked IID candidates

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
076638ec-85bd-4665-afc4-0af0c73076beff6811b0-d845-4d77-8edd-aaaa3d62ce992021-12-06WarningsExact identifier
spl id: 076638ec-85bd-4665-afc4-0af0c73076be
spl set id: ff6811b0-d845-4d77-8edd-aaaa3d62ce99

Reported adverse events (FAERS/openFDA)#

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