Label: SENNOSIDES tablet, film coated
- NDC Code(s): 0904-7252-60, 0904-7252-61, 0904-7252-80
- Packager: Major Pharmaceuticals
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated May 17, 2022
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- 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
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Directions
take preferably at bedtime or as directed by a doctor
age starting dosage maximum dosage adults and children 12
years of age and over2 tablets once
a day4 tablets twice
a daychildren 6 to under
12 years1 tablet once
a day2 tablets twice
a daychildren 2 to under
6 years1/2 tablet once
a day1 tablet twice
a daychildren under
2 yearsask a doctor ask a doctor - Other information
- INACTIVE INGREDIENT
- Questions or comments?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
SENNOSIDES
sennosides tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0904-7252 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 DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP) HYPROMELLOSES (UNII: 3NXW29V3WO) TALC (UNII: 7SEV7J4R1U) MALTODEXTRIN (UNII: 7CVR7L4A2D) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) LIGHT MINERAL OIL (UNII: N6K5787QVP) MAGNESIUM STEARATE (UNII: 70097M6I30) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) Product Characteristics Color brown Score no score Shape ROUND Size 9mm Flavor Imprint Code W2 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0904-7252-60 100 in 1 BOTTLE; Type 0: Not a Combination Product 05/17/2022 2 NDC:0904-7252-80 1000 in 1 BOTTLE; Type 0: Not a Combination Product 05/17/2022 3 NDC:0904-7252-61 10 in 1 BOX, UNIT-DOSE 05/17/2022 3 10 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 not final part334 05/17/2022 Labeler - Major Pharmaceuticals (191427277)