Label: SENNA LAXATIVE- sennosides tablet
- NDC Code(s): 0761-0798-02
- Packager: Basic Drugs, Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated May 7, 2024
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- Official Label (Printer Friendly)
- Active ingredient (in each tablet)
- Purpose
- Uses
-
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 continues 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.
-
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 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?
- Package Label
-
INGREDIENTS AND APPEARANCE
SENNA LAXATIVE
sennosides tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0761-0798 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) ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J) HYPROMELLOSES (UNII: 3NXW29V3WO) MINERAL OIL (UNII: T5L8T28FGP) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) 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:0761-0798-02 100 in 1 BOTTLE; Type 0: Not a Combination Product 05/07/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 05/07/2024 Labeler - Basic Drugs, Inc. (052155082)