Label: SENNOSIDES tablet, film coated
- NDC Code(s): 70000-0447-1, 70000-0447-2, 70000-0447-3
- Packager: Cardinal Health
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 22, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- PURPOSE
- Uses
-
WARNINGS
Ask a doctor before use if you have
■ stomach pain
■ nausea
■ vomiting
■ noticed a sudden change in bowel habits that continues over a period of 2 weeks
-
Directions
■ take preferably at bedtime or as directed by a doctor
Age Starting Dosage Maximum Dosage adults and children 12 years of age
and over
2 tablets once a day
4 tablet twice a day
children 6 to under 12 years
1 tablets once a day
2 tablets once 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
- INACTIVE INGREDIENT
- Questions or comments?
-
SPL UNCLASSIFIED SECTION
†This product is not manufactured or distributed by Purdue Products L.P., owner of the registered trademark Senokot®.
TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING.
DISTRIBUTED BY CARDINAL HEALTH
DUBLIN, OHIO 43017
www.myleader.com 1-800-200-6313
© 2018 Cardinal Health. All Rights Reserved. CARDINAL HEALTH,
the Cardinal Health LOGO, LEADER, and the Leader LOGO are
trademarks or registered trademarks of Cardinal Health. All
other marks are the property of their respective owners.
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- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
SENNOSIDES
sennosides tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70000-0447 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 POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) HYPROMELLOSES (UNII: 3NXW29V3WO) MAGNESIUM STEARATE (UNII: 70097M6I30) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) LIGHT MINERAL OIL (UNII: N6K5787QVP) TALC (UNII: 7SEV7J4R1U) MALTODEXTRIN (UNII: 7CVR7L4A2D) DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP) Product Characteristics Color brown Score no score Shape ROUND Size 9mm Flavor Imprint Code 1122;1122 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70000-0447-1 250 in 1 BOTTLE; Type 0: Not a Combination Product 11/14/2018 2 NDC:70000-0447-2 50 in 1 BOTTLE; Type 0: Not a Combination Product 01/04/2019 3 NDC:70000-0447-3 1 in 1 CARTON 04/27/2020 3 100 in 1 BOTTLE; 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 11/14/2018 Labeler - Cardinal Health (063997360)