Label: SENOKOT- standardized senna concentrate tablet, film coated
- NDC Code(s): 67618-120-06, 67618-120-12, 67618-120-36
- Packager: Atlantis Consumer Healthcare, Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 26, 2023
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- WHEN USING
- WARNINGS
- DO NOT USE
- ASK DOCTOR
- STOP USE
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- DOSAGE FORMS & STRENGTHS
- QUESTIONS
- INACTIVE INGREDIENT
- INDICATIONS & USAGE
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
SENOKOT
standardized senna concentrate tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:67618-120 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SENNOSIDES (UNII: 3FYP5M0IJX) (SENNOSIDES - UNII:3FYP5M0IJX) SENNOSIDES 17.2 mg Inactive Ingredients Ingredient Name Strength CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) TARTARIC ACID (UNII: W4888I119H) DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP) LIGHT MINERAL OIL (UNII: N6K5787QVP) TALC (UNII: 7SEV7J4R1U) STEARIC ACID (UNII: 4ELV7Z65AP) Product Characteristics Color BROWN (Light Brown) Score no score Shape ROUND Size 9mm Flavor Imprint Code X Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:67618-120-12 1 in 1 CARTON 09/01/1988 1 12 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:67618-120-36 3 in 1 CELLO PACK 09/01/1988 01/01/2023 2 12 in 1 BLISTER PACK 2 12 in 1 BLISTER PACK; Type 0: Not a Combination Product 3 NDC:67618-120-06 36 in 1 BOTTLE; Type 0: Not a Combination Product 09/01/1988 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M007 09/01/1988 Labeler - Atlantis Consumer Healthcare, Inc. (118983925) Registrant - Atlantis Consumer Healthcare, Inc. (118983925)