Label: STOOL SOFTENER LAXATIVE EXTRA STRENGTH- docusate sodium capsule, liquid filled
- NDC Code(s): 79903-073-14
- Packager: WALMART INC. (see also Equate)
- 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 February 9, 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
- Product Label
-
INGREDIENTS AND APPEARANCE
STOOL SOFTENER LAXATIVE EXTRA STRENGTH
docusate sodium capsule, liquid filledProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79903-073 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, UNSPECIFIED (UNII: 3WJQ0SDW1A) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SORBITOL (UNII: 506T60A25R) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) ISOPROPYL ALCOHOL (UNII: ND2M416302) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) MANNITOL (UNII: 3OWL53L36A) MINERAL OIL (UNII: T5L8T28FGP) SORBITAN (UNII: 6O92ICV9RU) Product Characteristics Color orange Score no score Shape CAPSULE Size 20mm Flavor Imprint Code P4 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79903-073-14 140 in 1 BOTTLE; Type 0: Not a Combination Product 06/25/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part334 06/25/2021 Labeler - WALMART INC. (see also Equate) (051957769)