Label: STOOL SOFTENER LAXATIVE- docusate sodium capsule, liquid filled
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NDC Code(s):
71335-9731-0,
71335-9731-1,
71335-9731-2,
71335-9731-3, view more71335-9731-4, 71335-9731-5, 71335-9731-6, 71335-9731-7, 71335-9731-8, 71335-9731-9
- Packager: Bryant Ranch Prepack
- This is a repackaged label.
- Source NDC Code(s): 0904-7280
- 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
- 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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HOW SUPPLIED
Docusate Sodium 100 mg
NDC: 71335-9731-1: 30 Tablets in a BOTTLE
NDC: 71335-9731-2: 100 Tablets in a BOTTLE
NDC: 71335-9731-3: 60 Tablets in a BOTTLE
NDC: 71335-9731-4: 120 Tablets in a BOTTLE
NDC: 71335-9731-5: 90 Tablets in a BOTTLE
NDC: 71335-9731-6: 180 Tablets in a BOTTLE
NDC: 71335-9731-7: 10 Tablets in a BOTTLE
NDC: 71335-9731-8: 28 Tablets in a BOTTLE
NDC: 71335-9731-9: 56 Tablets in a BOTTLE
NDC: 71335-9731-0: 18 Tablets 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 LAXATIVE
docusate sodium capsule, liquid filledProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71335-9731(NDC:0904-7280) 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, UNSPECIFIED (UNII: 2G86QN327L) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SORBITOL (UNII: 506T60A25R) GLYCERIN (UNII: PDC6A3C0OX) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SORBITAN (UNII: 6O92ICV9RU) Product Characteristics Color red Score no score Shape CAPSULE (Oval) Size 13mm Flavor Imprint Code PC1 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71335-9731-1 30 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/18/2023 2 NDC:71335-9731-2 100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/09/2023 3 NDC:71335-9731-3 60 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/17/2023 4 NDC:71335-9731-4 120 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/30/2024 5 NDC:71335-9731-5 90 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/17/2023 6 NDC:71335-9731-6 180 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/30/2024 7 NDC:71335-9731-7 10 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/30/2024 8 NDC:71335-9731-8 28 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/30/2024 9 NDC:71335-9731-9 56 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/30/2024 10 NDC:71335-9731-0 18 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 11/15/2022 Labeler - Bryant Ranch Prepack (171714327) Registrant - Bryant Ranch Prepack (171714327) Establishment Name Address ID/FEI Business Operations Bryant Ranch Prepack 171714327 REPACK(71335-9731) , RELABEL(71335-9731)