Label: EX-LAX MAXIMUM STRENGTH STIMULANT LAXATIVE
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- NDC Code(s): 0067-8142-01, 0067-8142-02
- Packager: Haleon US Holdings LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 17, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each tablet)
Sennosides 25 mg
- Purpose
Stimulant laxative
- Uses • relieves occasional constipation (irregularity) • generally produces bowel movement in 6 to 12 hours
- Warnings
Do Not Use
laxative products when abdominal pain, nausea, or vomiting are present unless directed by a doctor
Ask a doctor before use if you have
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
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
do not use for a period longer than 1 week
Stop use and ask a doctor if
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,
ask a health professional before use.
Keep Out of Reach of Children.
In case of overdose, get medical help or contact a Poison Control Center right away.
- Directions • swallow tablet(s) with a glass of water • swallow tablet(s) whole, do not crush, break or chew
adults and children 12 years of age and older
2 tablets once or twice daily
children 6 to under 12 years of age
1 tablet once or twice daily
children under 6 years of age
ask a doctor
- Other information • each tablet contains: calcium 40 mg, magnesium 5 mg • store at controlled room temperature 20-25C (68-77F).
- Inactive ingredients
acacia, calcium carbonate, carnauba wax, corn starch dibasic calcium phosphate, FD&C blue no.1 aluminum lake, iron oxide black, magnesium stearate, methyl paraben, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, povidone, propylene glycol, propylparaben, shellac, silicon dioxide, sodium benzoate, sodium lauryl sulfate, sucrose, talc, titanium dioxide
- Questions or Comments?
call 1-855-221-5432
- Additional information listed on other panels
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 GSK, attention Consumer Affairs, for full refund.
Tamper Evident Feature: Ex•Lax® Tablets are sealed in blister packets. Use only if the individual seal is unbroken.
- Principal Display Panel
MAXIMUM STRENGTH
ex•lax
SENNOSIDES, 25 mg
STIMULANT LAXATIVE
RELIEF GUARANTEED
24 TABLETS
GENTLE OVERNIGHT RELIEF YOU CAN TRUST
- INGREDIENTS AND APPEARANCE
EX-LAX MAXIMUM STRENGTH STIMULANT LAXATIVE sennosides pill Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0067-8142 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SENNOSIDES (UNII: 3FYP5M0IJX) (SENNOSIDES - UNII:3FYP5M0IJX) SENNOSIDES 25 mg Inactive Ingredients Ingredient Name Strength ACACIA (UNII: 5C5403N26O) CALCIUM CARBONATE (UNII: H0G9379FGK) CARNAUBA WAX (UNII: R12CBM0EIZ) STARCH, CORN (UNII: O8232NY3SJ) ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) ALUMINUM OXIDE (UNII: LMI26O6933) FERROSOFERRIC OXIDE (UNII: XM0M87F357) MAGNESIUM STEARATE (UNII: 70097M6I30) METHYLPARABEN (UNII: A2I8C7HI9T) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P) POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PROPYLPARABEN (UNII: Z8IX2SC1OH) SHELLAC (UNII: 46N107B71O) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM LAURYL SULFATE (UNII: 368GB5141J) SUCROSE (UNII: C151H8M554) TALC (UNII: 7SEV7J4R1U) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color BLUE Score no score Shape ROUND Size 10mm Flavor Imprint Code ex;lax;1 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0067-8142-01 2 in 1 CARTON 07/01/2017 1 12 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:0067-8142-02 4 in 1 CARTON 07/01/2017 2 12 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M007 07/01/2017 Labeler - Haleon US Holdings LLC (079944263)
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EX-LAX MAXIMUM STRENGTH STIMULANT LAXATIVE- sennosides pill
Number of versions: 6
| Published Date (What is this?) | Version | Files |
|---|---|---|
| Dec 19, 2024 | 6 (current) | download |
| Mar 15, 2024 | 5 | download |
| Dec 4, 2020 | 4 | download |
| Mar 12, 2019 | 3 | download |
| Mar 6, 2019 | 2 | download |
| Jul 3, 2017 | 1 | download |
EX-LAX MAXIMUM STRENGTH STIMULANT LAXATIVE- sennosides pill
| RxCUI | RxNorm NAME | RxTTY | |
|---|---|---|---|
| 1 | 213073 | Ex-Lax Maximum Strength 25 MG Oral Tablet | PSN |
| 2 | 213073 | sennosides, USP 25 MG Oral Tablet [Ex-Lax Maximum Relief Formula] | SBD |
| 3 | 213073 | Ex-Lax Maximum Relief Formula 25 MG Oral Tablet | SY |
| 4 | 251292 | sennosides 25 MG Oral Tablet | PSN |
| 5 | 251292 | sennosides, USP 25 MG Oral Tablet | SCD |
EX-LAX MAXIMUM STRENGTH STIMULANT LAXATIVE- sennosides pill
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EX-LAX MAXIMUM STRENGTH STIMULANT LAXATIVE- sennosides pill
If this SPL contains inactivated NDCs listed by the FDA initiated compliance action, they will be specified as such.
| NDC | |
|---|---|
| 1 | 0067-8142-01 |
| 2 | 0067-8142-02 |
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