Label: DOCUSATE SODIUM capsule, liquid filled
- NDC Code(s): 50268-268-11, 50268-268-15
- Packager: AvPAK
- This is a repackaged label.
- Source NDC Code(s): 54629-601
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 31, 2023
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 softgel)
- Purpose
- Keep Out of Reach of Children.
- Uses
- Warnings
- Ask a doctor before use
- Stop use and ask a doctor
- If you are pregnant or breast-feeding,
- Directions
- Other Information
- Inactive ingredients
- Questions
- Package/Label Principal Display Panel
-
INGREDIENTS AND APPEARANCE
DOCUSATE SODIUM
docusate sodium capsule, liquid filledProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50268-268(NDC:54629-601) Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DOCUSATE SODIUM (UNII: F05Q2T2JA0) (DOCUSATE - UNII:M7P27195AG) DOCUSATE SODIUM 250 mg Inactive Ingredients Ingredient Name Strength FD&C RED NO. 40 (UNII: WZB9127XOA) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) GELATIN (UNII: 2G86QN327L) GLYCERIN (UNII: PDC6A3C0OX) POLYETHYLENE GLYCOL 1000 (UNII: U076Q6Q621) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SORBITOL (UNII: 506T60A25R) Product Characteristics Color red Score no score Shape OVAL Size 20mm Flavor Imprint Code NV12 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50268-268-15 50 in 1 BOX 05/17/2017 1 NDC:50268-268-11 1 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M007 05/17/2017 Labeler - AvPAK (832926666)