Label: SENNA LAXATIVE- sennosides tablet
- NDC Code(s): 70677-1247-1
- Packager: Strategic Sourcing Services LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 6, 2024
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient (in each tablet) Sennosides 8.6 mg
- Purpose Laxative
- Uses • relieves occasional constipation (irregularity) • generally produces bowel movement in 6-12 hours
- Warnings Do not use • 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 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 (1-800-222-1222) right away.
- Directions• take preferbly 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 ½ tablet once a day tablets twice a day children 2 years ask a doctor ask a doctor
- Other information
- Inactive ingredients Colloidal silicon dioxide, croscarmellose sodium, dicalcium phosphate, hypromellose, liquid paraffin, magnesium stearate, microcrystalline cellulose, maltodextrin, purified water, sodium lauryl sulphate, stearic acid
- Questions or comments?833-358-6431
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INGREDIENTS AND APPEARANCE
SENNA LAXATIVE
sennosides tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70677-1247 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SENNOSIDES (UNII: 3FYP5M0IJX) (SENNOSIDES - UNII:3FYP5M0IJX) SENNOSIDES 8.6 mg Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: L11K75P92J) PARAFFIN (UNII: I9O0E3H2ZE) MAGNESIUM STEARATE (UNII: 70097M6I30) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) MALTODEXTRIN (UNII: 7CVR7L4A2D) WATER (UNII: 059QF0KO0R) SODIUM LAURYL SULFATE (UNII: 368GB5141J) STEARIC ACID (UNII: 4ELV7Z65AP) Product Characteristics Color brown Score no score Shape ROUND Size 9mm Flavor Imprint Code S8 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70677-1247-1 150 in 1 BOTTLE; Type 0: Not a Combination Product 02/06/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M007 02/06/2024 Labeler - Strategic Sourcing Services LLC (116956644)
