Label: STOOL SOFTENER LAXATIVE- docusate sodium capsule
- NDC Code(s): 41163-862-25
- Packager: United Natural Foods, Inc. dba UNFI
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated May 23, 2024
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- Official Label (Printer Friendly)
- Active ingredient (in each softgel)
- Purpose
- Uses
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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?
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Principal Display Panel
compare to Dulcolax® Stool Softener active ingredient†
stool softener
docusate sodium 100 mg
stool softener laxative
- comfortable relief of painful, hard, dry stool
- stimulant-free
- constipation relief
Softgels
†This product is not manufactured or distributed by Chattem, Inc., distributor of Dulcolax® Stool Softener
TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING.
KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION.
DISTRIBUTED BY UNFI
PROVIDENCE, RI 02908 USA
- Product Label
-
INGREDIENTS AND APPEARANCE
STOOL SOFTENER LAXATIVE
docusate sodium capsuleProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41163-862 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) Product Characteristics Color orange Score no score Shape OVAL Size 12mm Flavor Imprint Code P51 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41163-862-25 1 in 1 BOX 01/31/2020 1 25 in 1 BOTTLE, PLASTIC; 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 01/31/2020 Labeler - United Natural Foods, Inc. dba UNFI (943556183)