Label: STOOL SOFTENER- docusate sodium capsule, liquid filled
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NDC Code(s):
71335-9738-1,
71335-9738-2,
71335-9738-3,
71335-9738-4, view more71335-9738-5
- Packager: Bryant Ranch Prepack
- This is a repackaged label.
- Source NDC Code(s): 0904-6999
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated May 30, 2024
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
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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HOW SUPPLIED
Docusate Sodium 250 mg
NDC: 71335-9738-1: 30 Capsules in a BOTTLE
NDC: 71335-9738-2: 60 Capsules in a BOTTLE
NDC: 71335-9738-3: 100 Capsules in a BOTTLE
NDC: 71335-9738-4: 7 Capsules in a BOTTLE
NDC: 71335-9738-5: 90 Capsules in a BOTTLE
Repackaged/Relabeled by:
Bryant Ranch Prepack, Inc.
Burbank, CA 91504 - PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
STOOL SOFTENER
docusate sodium capsule, liquid filledProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71335-9738(NDC:0904-6999) 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, UNSPECIFIED (UNII: 2G86QN327L) GLYCERIN (UNII: PDC6A3C0OX) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SORBITOL (UNII: 506T60A25R) MANNITOL (UNII: 3OWL53L36A) SORBITAN (UNII: 6O92ICV9RU) Product Characteristics Color orange Score no score Shape CAPSULE Size 20mm Flavor Imprint Code P20 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71335-9738-1 30 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/26/2023 2 NDC:71335-9738-2 60 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/21/2023 3 NDC:71335-9738-3 100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/30/2024 4 NDC:71335-9738-4 7 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/20/2023 5 NDC:71335-9738-5 90 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/30/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M007 09/30/2019 Labeler - Bryant Ranch Prepack (171714327) Registrant - Bryant Ranch Prepack (171714327) Establishment Name Address ID/FEI Business Operations Bryant Ranch Prepack 171714327 REPACK(71335-9738) , RELABEL(71335-9738)