Label: SENNOSIDES, DOCUSATE SODIUM tablet, film coated
-
NDC Code(s):
10267-5609-1,
10267-5609-4,
10267-5609-5,
10267-5609-6, view more10267-5609-7
- Packager: Contract Pharmacal Corp.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Export only
Drug Label Information
Updated March 24, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
SENNOSIDES, DOCUSATE SODIUM
sennosides, docusate sodium tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10267-5609 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DOCUSATE SODIUM (UNII: F05Q2T2JA0) (DOCUSATE - UNII:M7P27195AG) DOCUSATE SODIUM 50 mg SENNOSIDES (UNII: 3FYP5M0IJX) (SENNOSIDES - UNII:3FYP5M0IJX) SENNOSIDES 8.6 mg Inactive Ingredients Ingredient Name Strength FD&C YELLOW NO. 6 (UNII: H77VEI93A8) GUAR GUM (UNII: E89I1637KE) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) POLYETHYLENE GLYCOL 4000 (UNII: 4R4HFI6D95) POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990) TALC (UNII: 7SEV7J4R1U) SODIUM BENZOATE (UNII: OJ245FE5EU) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) STARCH, CORN (UNII: O8232NY3SJ) D&C YELLOW NO. 10 ALUMINUM LAKE (UNII: CQ3XH3DET6) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) Product Characteristics Color orange Score no score Shape ROUND Size 9mm Flavor Imprint Code SS Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10267-5609-5 1 in 1 CARTON 11/16/2020 1 120 in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:10267-5609-7 1 in 1 CARTON 11/17/2020 2 60 in 1 BOTTLE; Type 0: Not a Combination Product 3 NDC:10267-5609-6 1 in 1 CARTON 05/07/2021 3 20 in 1 BOTTLE; Type 0: Not a Combination Product 4 NDC:10267-5609-1 1 in 1 CARTON 11/04/2021 4 10 in 1 BLISTER PACK; Type 0: Not a Combination Product 5 NDC:10267-5609-4 1000 in 1 BOTTLE; Type 0: Not a Combination Product 08/25/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Export only 11/16/2020 Labeler - Contract Pharmacal Corp. (057795122) Registrant - Contract Pharmacal Corp. (057795122) Establishment Name Address ID/FEI Business Operations Contract Pharmacal Corp. 057795122 pack(10267-5609) , label(10267-5609) Establishment Name Address ID/FEI Business Operations Contract Pharmacal Corp. 078666313 label(10267-5609) , pack(10267-5609) Establishment Name Address ID/FEI Business Operations Contract Pharmacal Corp. 079157508 manufacture(10267-5609) Establishment Name Address ID/FEI Business Operations Contract Pharmacal Corp. 968334974 manufacture(10267-5609) Establishment Name Address ID/FEI Business Operations Contract Pharmacal Corp. 968335112 manufacture(10267-5609)
