Label: DOK- docusate sodium capsule
- NDC Code(s): 0904-6457-60, 0904-6457-80
- Packager: Major Pharmaceuticals
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 27, 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
- Uses
-
Warnings
Ask a doctor before use if you have
- stomach pain
- nausea
- vomiting
- noticed a sudden change in bowel habits that last over 2 weeks
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
-
Principal Display Panel
Compare to the active ingredient in Colace® Regular Strength Stool Softener**
DOK™ 100 mg
Docusate sodium
Stool Softener Laxative
For Use as a Stool Softener in Treating & Avoiding Constipation
Softgels
**This product is not manufactured or distributed bt Purdue Products L.P., distributor of Colace® Regular Strength Stool Softener.
TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING.
Distributed by:
Major® Pharmaceuticals
17177 N Laurel Park Drive, Suite 233
Livonia, MI 48152
- Product Label
-
INGREDIENTS AND APPEARANCE
DOK
docusate sodium capsuleProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0904-6457 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DOCUSATE SODIUM (UNII: F05Q2T2JA0) (DOCUSATE - UNII:M7P27195AG) DOCUSATE SODIUM 100 mg Inactive Ingredients Ingredient Name Strength FD&C RED NO. 40 (UNII: WZB9127XOA) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) GELATIN (UNII: 2G86QN327L) SORBITAN (UNII: 6O92ICV9RU) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SORBITOL (UNII: 506T60A25R) GLYCERIN (UNII: PDC6A3C0OX) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) Product Characteristics Color orange Score no score Shape OVAL Size 12mm Flavor Imprint Code P51;S77;SCU1;D2 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0904-6457-60 100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/28/2015 12/28/2023 2 NDC:0904-6457-80 1000 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/28/2015 12/28/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M007 02/28/2015 12/28/2023 Labeler - Major Pharmaceuticals (191427277)