Label: SENNA LAXATIVE- sennosides tablet, film coated
- NDC Code(s): 55910-208-12
- Packager: DOLGENCORP, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 10, 2024
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active ingredient (in each tablet)
- Purpose
- Uses
- Warnings
-
Directions
- take preferably at bedtime or as directed by a doctor
age starting dosage maximum dosage adults and children 12 years and 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
- Inactive ingredients
- Questions or comments?
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Principal display panel
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Compare to
active ingredient
of Senokot®*Vegetable Laxative Ingredient
Gentle, Overnight ReliefRegular Strength
Senna Laxative
Sennosides USP, 8.6 mg/Stimulant Laxative
- Vegetable Laxative Ingredient
- Gentle, Overnight Relief
8.6
mg each100 Tablets
Actual Tablet Size*This product is not manufactured or distributed by
Atlantis Consumer Healthcare Inc., owner of the registered
trademark Senokot®. 50844 ORG102029812TAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY
SEAL UNDER CAP IS BROKEN OR MISSINGDISTRIBUTED BY
OLD EAST MAIN CO.
100 MISSION RIDGE
GOODLETTSVILLE, TN 37072Dollar general 44-298
-
INGREDIENTS AND APPEARANCE
SENNA LAXATIVE
sennosides tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55910-208 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 CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) Product Characteristics Color brown Score no score Shape ROUND Size 9mm Flavor Imprint Code 44;298 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55910-208-12 1 in 1 CARTON 04/10/2024 1 100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 04/10/2024 Labeler - DOLGENCORP, LLC (068331990) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 pack(55910-208) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(55910-208) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867894 manufacture(55910-208) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 pack(55910-208) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 117025878 manufacture(55910-208)