EX-LAX

Manufacturer
Haleon US Holdings LLC
Effective date
2024-12-17
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 00:44:12

Label at a glance#

ProductEX-LAX REGULAR STRENGTH CHOCOLATED STIMULANT LAXATIVE
Active ingredientSENNOSIDES
Label structure10 sections

Indications and uses

• relieves occasional constipation (irregularity) • generally produces bowel movement in 6 to 12 hours

Dosage and administration

adults and children 12 years of age and older chew 2 chocolated pieces once or twice daily children 6 to under 12 years of age chew 1 chocolated piece once or twice daily children under 6 years of age ask a doctor

Storage and handling

• each piece contains: potassium 10 mg • store at 15-25 o C (59-77 o F)

Label contents#

Full prescribing information#

Active ingredient (in each piece)

OTC - ACTIVE INGREDIENT SECTION

Sennosides 15 mg

Purpose

OTC - PURPOSE SECTION

Stimulant laxative

Uses

INDICATIONS & USAGE SECTION

  • relieves occasional constipation (irregularity)
  • generally produces bowel movement in 6 to 12 hours

Warnings

WARNINGS SECTION

Do not use

OTC - DO NOT USE SECTION

laxative products when abdominal pain, nausea or vomiting are present unless directed by a doctor

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

noticed a sudden change in bowel habits that persists over a period of 2 weeks

Ask a doctor or pharmacist before use if you are

OTC - ASK DOCTOR/PHARMACIST SECTION

taking any other drug. Laxatives may affect how other drugs work. Take this product 2 or more hours before or after other drugs.

When using this product

OTC - WHEN USING SECTION

do not use for a period longer than 1 week

Stop use and ask a doctor if

OTC - STOP USE SECTION

rectal bleeding or failure to have a bowel movement occur after use of a laxative. These may be signs of a serious condition.

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

adults and children 12 years of age and older

chew 2 chocolated pieces once or twice daily

children 6 to under 12 years of age

chew 1 chocolated piece once or twice daily

children under 6 years of age

ask a doctor

Other information

STORAGE AND HANDLING SECTION

  • each piece contains: potassium 10 mg
  • store at 15-25oC (59-77oF)

Inactive ingredients

INACTIVE INGREDIENT SECTION

cocoa powder, hydrogenated vegetable oils (palm kernel, palm), salt, soy lecithin, sugar, vanilla, whey powder (milk)

Questions or comments?

OTC - QUESTIONS SECTION

call 1-855-221-5432

Generic Section

SPL UNCLASSIFIED SECTION

Tamper Evident Feature: Do not use if carton or inner foil wrapping is damaged or open.

The Ex-Lax Guarantee: When taken as directed, Ex-Lax is guaranteed to work gently and effectively overnight or your money back. Return product to Haleon, attention Consumer Affairs, for full refund.

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

REGULAR STRENGTH

ex-lax

Sennosides, 15 mg

Chocolated Stimulant Laxative

Relief Guaranteed

48 PIECES

GENTLE OVERNIGHT RELIEF YOU CAN TRUST

Ex-Lax Choco Reg Strength 48 ct
Ex-Lax Choco Reg Strength 48 ct

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
213071Ex-Lax Regular Strength Chocolated 15 MG Chewable TabletPSN6
251020sennosides 15 MG Chewable TabletPSN6
213071sennosides, USP 15 MG Chewable Tablet [Ex-Lax Chocolated]SBD6
251020sennosides, USP 15 MG Chewable TabletSCD6
213071Ex-Lax Chocolated 15 MG Chewable TabletSY6

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0067-8140-01EX-LAXREGULAR STRENGTH CHOCOLATED STIMULANT LAXATIVE12 in 1 PACKAGETABLET, CHEWABLE126
0067-8140-01EX-LAXREGULAR STRENGTH CHOCOLATED STIMULANT LAXATIVE1 in 1 BOXTABLET, CHEWABLE16
0067-8140-02EX-LAXREGULAR STRENGTH CHOCOLATED STIMULANT LAXATIVE2 in 1 BOXTABLET, CHEWABLE26
0067-8140-02EX-LAXREGULAR STRENGTH CHOCOLATED STIMULANT LAXATIVE12 in 1 PACKAGETABLET, CHEWABLE126
0067-8140-03EX-LAXREGULAR STRENGTH CHOCOLATED STIMULANT LAXATIVE12 in 1 PACKAGETABLET, CHEWABLE126
0067-8140-03EX-LAXREGULAR STRENGTH CHOCOLATED STIMULANT LAXATIVE4 in 1 BOXTABLET, CHEWABLE46

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0067-8140EX-LAX REGULAR STRENGTH CHOCOLATED STIMULANT LAXATIVE (SENNOSIDES) TABLET, CHEWABLE [HALEON US HOLDINGS LLC]6Current NDC, Legacy NDC, 6 package rows20241219_59a26a7f-516f-4507-8dec-f40cf6cfaffc.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0067-8140-01EA - Each0067-8140ef645ac1-a019-404b-9c71-1bf42c10702412025-05-14
0067-8140-02EA - Each0067-8140dbe00176-bc5b-4c64-8e5a-7e5959799d5c12020-04-20
0067-8140-03EA - Each0067-81407695f527-3920-488e-97a5-76861ba357bf12024-11-05

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0067-81400067-8140-01, 0067-8140-02, 0067-8140-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

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
EX-LAX REGULAR STRENGTH CHOCOLATED STIMULANT LAXATIVESENNOSIDESHaleon US Holdings LLC59a26a7f-516f-4507-8dec-f40cf6cfaffc2024-12-17WarningsExact identifier
ndc (package): 0067-8140-02
ndc (package): 0067-8140-01
ndc (package): 0067-8140-03
ndc (product): 0067-8140
ndc11 (package): 00067814001
ndc11 (package): 00067814002
ndc11 (package): 00067814003
spl id: 0add1e20-57d2-4642-81ab-a356989ea677
spl set id: 59a26a7f-516f-4507-8dec-f40cf6cfaffc

Reported adverse events (FAERS/openFDA)#

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