Label: MAXIMUM STRENGTH SENNA LAXATIVE- sennoside 25 mg tablet
- NDC Code(s): 72090-016-01
- Packager: Pioneer Life Sciences, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 10, 2025
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient (in each tablet)
- Purpose
- Uses:
- Warnings:
- ASK DOCTOR
- WHEN USING
- STOP USE
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- DIRECTIONS
- OTHER INFORMATION
-
INACTIVE INGREDIENTS
Microcrystalline Cellulose, Dicalcium Phosphate/Dibasic Calcium Phosphate, Croscarmellose Sodium, Sodium Lauryl sulphate, Colloidal Silicon Dioxide, Crospovidone, Stearic acid powder, Magnesium Stearate, Brilliant Blue Lake, Indigo Carmine Lake, Polyvinly Alcohol, Polyethylene Glycol, Titanium Dioxide, Talc
- QUESTIONS OR COMMENTS?
- NDC 72090-016-01 (100ct Bottle)
-
INGREDIENTS AND APPEARANCE
MAXIMUM STRENGTH SENNA LAXATIVE
sennoside 25 mg tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72090-016 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SENNOSIDES (UNII: 3FYP5M0IJX) (SENNOSIDES - UNII:3FYP5M0IJX) SENNOSIDES 25 mg Inactive Ingredients Ingredient Name Strength MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) SODIUM LAURYL SULFATE (UNII: 368GB5141J) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) CROSPOVIDONE, UNSPECIFIED (UNII: 2S7830E561) STEARIC ACID (UNII: 4ELV7Z65AP) MAGNESIUM STEARATE (UNII: 70097M6I30) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) INDIGOTINDISULFONATE SODIUM (UNII: D3741U8K7L) POLYVINYL ALCOHOL (UNII: 532B59J990) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) TALC (UNII: 7SEV7J4R1U) Product Characteristics Color blue (Light Blue) Score no score Shape ROUND (Biconvex) Size 11mm Flavor Imprint Code S3 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72090-016-01 100 in 1 BOTTLE; Type 0: Not a Combination Product 03/06/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 03/06/2025 Labeler - Pioneer Life Sciences, LLC (014092742) Registrant - Pioneer Life Sciences, LLC (014092742)