Label: DOCUSATE SODIUM- docusate sodium 100mg capsule
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Contains inactivated NDC Code(s)
NDC Code(s): 50090-2731-0, 50090-2731-1, 50090-2731-2, 50090-2731-4 - Packager: A-S Medication Solutions
- This is a repackaged label.
- Source NDC Code(s): 16103-399
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated April 25, 2019
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
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Warnings
Do not use if you are presently taking mineral oil, unless told to do so by a doctor
Ask a doctor before use if you have
- stomach pain
- nausea
- vomiting
- noticed a sudden change in bowel habits that lasts over 2 weeks
- Directions
- Other information
- Inactive ingredients
- Questions?
- HOW SUPPLIED
- Docusate Sodium 100mg
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INGREDIENTS AND APPEARANCE
DOCUSATE SODIUM
docusate sodium 100mg capsuleProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50090-2731(NDC:16103-399) 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 D&C RED NO. 33 (UNII: 9DBA0SBB0L) FD&C Red No. 40 (UNII: WZB9127XOA) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) GELATIN, UNSPECIFIED (UNII: 2G86QN327L) GLYCERIN (UNII: PDC6A3C0OX) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) WATER (UNII: 059QF0KO0R) SORBITOL (UNII: 506T60A25R) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color red (Two-toned- white and clear red) Score no score Shape OVAL Size 12mm Flavor Imprint Code SCU2 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50090-2731-1 100 in 1 BOTTLE; Type 0: Not a Combination Product 12/28/2016 2 NDC:50090-2731-2 60 in 1 BOTTLE; Type 0: Not a Combination Product 12/29/2016 3 NDC:50090-2731-4 30 in 1 BOTTLE; Type 0: Not a Combination Product 04/04/2017 4 NDC:50090-2731-0 20 in 1 BOTTLE; Type 0: Not a Combination Product 03/22/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part334 03/01/2016 Labeler - A-S Medication Solutions (830016429) Establishment Name Address ID/FEI Business Operations A-S Medication Solutions 830016429 RELABEL(50090-2731) , REPACK(50090-2731)