Label: SENNA LAXATIVE tablet
- NDC Code(s): 72090-041-01, 72090-041-02
- Packager: Pioneer Life Sciences, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 6, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient (in each tablet)
- Purpose
- Uses:
- Warnings:
- ASK DOCTOR
- STOP USE
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
-
DIRECTIONS
- Take preferably at bedtime or as directed by a doctor.
age
starting dosage
maximum dosage
adults & 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 OR COMMENTS?
- NDC 72090-041-01 (300ct Bottle)
- NDC 72090-041-02 (600ct Bottle)
-
INGREDIENTS AND APPEARANCE
SENNA LAXATIVE
senna laxative tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72090-041 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 LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) CROSPOVIDONE, UNSPECIFIED (UNII: 2S7830E561) POVIDONE K30 (UNII: U725QWY32X) MAGNESIUM STEARATE (UNII: 70097M6I30) POLYVINYL ALCOHOL (UNII: 532B59J990) POLYSORBATE 80 (UNII: 6OZP39ZG8H) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) TALC (UNII: 7SEV7J4R1U) Product Characteristics Color brown Score no score Shape ROUND Size 10mm Flavor Imprint Code CS Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72090-041-01 300 in 1 BOTTLE; Type 0: Not a Combination Product 03/05/2025 2 NDC:72090-041-02 600 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) 03/05/2025 Labeler - Pioneer Life Sciences, LLC (014092742) Registrant - Pioneer Life Sciences, LLC (014092742)


