Label: SENNOSIDES tablet
- NDC Code(s): 72789-283-10, 72789-283-30
- Packager: PD-Rx Pharmaceuticals, Inc.
- This is a repackaged label.
- Source NDC Code(s): 69618-064
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated October 2, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient (in each tablet)
- Purpose
- Uses
- Warnings
- ASK DOCTOR
- STOP USE
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- Other information
- Inactive ingredients
- Questions or comments?
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Directions
take preferably at bedtime or as directed by a doctor
do not exceed maximum dosage
age starting dosage maximum dosage adults and children 12 years of age or older 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
- HOW SUPPLIED
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
SENNOSIDES
sennosides tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72789-283(NDC:69618-064) Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SENNOSIDES A AND B (UNII: 1B5FPI42EN) (SENNOSIDES A AND B - UNII:1B5FPI42EN) SENNOSIDES A AND B 8.6 mg Inactive Ingredients Ingredient Name Strength CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) MAGNESIUM STEARATE (UNII: 70097M6I30) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) Product Characteristics Color brown (light) Score no score Shape ROUND Size 9mm Flavor Imprint Code S5 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72789-283-10 10 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/22/2022 2 NDC:72789-283-30 30 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/24/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M007 08/01/2020 Labeler - PD-Rx Pharmaceuticals, Inc. (156893695) Registrant - PD-Rx Pharmaceuticals, Inc. (156893695) Establishment Name Address ID/FEI Business Operations PD-Rx Pharmaceuticals, Inc. 156893695 repack(72789-283)