Label: STOOL SOFTENER LAXATIVE- docusate sodium capsule, liquid filled
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Contains inactivated NDC Code(s)
NDC Code(s): 0363-0016-06, 0363-0016-20, 0363-0016-40 - Packager: Walgreens
- Category: HUMAN OTC DRUG LABEL
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 October 3, 2019
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- Download DRUG LABEL INFO: PDF XML
- 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 lasts over 2 weeks
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
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Principal Display Panel
Compare to the active ingredient in Colace® Regular Strength Stool Softener††
Stool Softener
DOCUSATE SODIUM 100 mg / STOOL SOFTENER LAXATIVE
REGULAR STRENGTH SOFTGELS
- Effective relief of constipation
- Gentle & dependable
- Stimulant free
SOFTGELS
††This product is not manufactured or distributed by 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
KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION
DISTRIBUTED BY: WALGREEN CO.
200 WILMOT RD., DEERFIELD, IL 60015
walgreens.com
- Product Label
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INGREDIENTS AND APPEARANCE
STOOL SOFTENER LAXATIVE
docusate sodium capsule, liquid filledProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0016 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 BLUE NO. 1 (UNII: H3R47K3TBD) FD&C RED NO. 40 (UNII: WZB9127XOA) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) GELATIN (UNII: 2G86QN327L) GLYCERIN (UNII: PDC6A3C0OX) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SORBITAN (UNII: 6O92ICV9RU) SORBITOL (UNII: 506T60A25R) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color RED, WHITE Score no score Shape OVAL Size 12mm Flavor Imprint Code P10;SCU2;D1 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0016-06 1 in 1 BOX 08/31/2017 1 60 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 2 NDC:0363-0016-20 1 in 1 BOX 08/31/2017 2 200 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 3 NDC:0363-0016-40 1 in 1 BOX 08/31/2017 3 400 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 NOT FINAL part334 08/31/2017 Labeler - Walgreens (008965063)