Label: SENNA-S- docusate sodium and sennosides tablet, film coated
- NDC Code(s): 70677-1246-1
- Packager: Strategic Sourcing Services, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 2, 2024
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredients (in each tablet) Docusate sodium 50 mg Sennosides 8.6 mg
- PurposeStool Softner Laxative
- Uses• relieves occasional constipation (irregularity) • generally produces bowel movement in 6-12 hours
- Warnings Do not use • If you are now taking mineral oil, unless directed by a doctor • laxative products for longer than 1 week, unless directed by a doctor
- Ask a doctor before use if you have• stomach pain • nausea • vomiting • noticed a sudden change in bowel habits that lasts over a period of 2 weeks
- Stop use and ask a doctor ifyou have rectal bleeding or fail to have a bowel movement after use of a laxative. These may indicate 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 1(800)222-1222
- Directions• take preferably at bedtime or as directed by a doctor Age Starting Dosage Maximum Dosage adults and children 12 years of age or over 2 tablets once a day 4 tablets twice a day children 6 to under 12 years 1 tablet once a day 2 tablets twice a day children 2 to under 6 years 1/2 tablet once a day 1 tablet twice a day children under 2 years ask a doctor ask a doctor
- Other information• each tablet contains:calcium 20 mg, sodium 6 mg • store at 25°C (77°F); excursions permitted between 15°-30°C (59°-86°F)
- Inactive ingredients: carnauba wax, colloidal silicon dioxide, croscarmellose sodium, dicalcium phosphate, D&C yellow No. 10, FD&C Yellow No. 6, hypromellose, magnesium stearate, microcrystalline cellulose, maltodextrin, polyethylene glycol, purified water, sodium benzoate, stearic acid, titanium dioxide
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INGREDIENTS AND APPEARANCE
SENNA-S
docusate sodium and sennosides tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70677-1246 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DOCUSATE SODIUM (UNII: F05Q2T2JA0) (DOCUSATE - UNII:M7P27195AG) DOCUSATE SODIUM 50 mg SENNOSIDES (UNII: 3FYP5M0IJX) (SENNOSIDES - UNII:3FYP5M0IJX) SENNOSIDES 8.6 mg Inactive Ingredients Ingredient Name Strength CARNAUBA WAX (UNII: R12CBM0EIZ) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP) D&C YELLOW NO. 10 (UNII: 35SW5USQ3G) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) HYPROMELLOSES (UNII: 3NXW29V3WO) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) MALTODEXTRIN (UNII: 7CVR7L4A2D) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) WATER (UNII: 059QF0KO0R) SODIUM BENZOATE (UNII: OJ245FE5EU) STEARIC ACID (UNII: 4ELV7Z65AP) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color orange Score no score Shape ROUND Size 10mm Flavor Imprint Code S;35 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70677-1246-1 100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/02/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M007 02/02/2024 Labeler - Strategic Sourcing Services, LLC (116956644)
