Label: STOOL SOFTENER LAXATIVE- docusate sodium and sennosides tablet
- NDC Code(s): 37808-355-12, 37808-355-24
- Packager: H E B
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated September 9, 2024
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- Official Label (Printer Friendly)
- Active ingredients (in each tablet)
- Purpose
- Uses
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Warnings
Do not use
- laxative products for longer than 1 week unless directed by a doctor
- if you are presently taking mineral oil, unless told to do so by a doctor
Ask a doctor before use if you have
- stomach pain
- nausea
- vomiting
- noticed a sudden change in bowel habits that lasts over a period of 2 weeks
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Directions
- take only by mouth. Doses may be taken as a single daily dose, preferably in the evening, or in divided doses.
adults and children 12 years and older take 2-4 tablets daily children 6 to under 12 years of age take 1-2 tablets daily children 2 to under 6 years of age take up to 1 tablet daily children under 2 ask a doctor
- Other information
- Inactive ingredients
- Questions or comments?
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Principal Display Panel
Compare to Colace® 2-IN1 Tablets active ingredients**
Stool Softener & Stimulant Laxative
Docusate sodium 50 mg
Sennosides 8.6 mg
Stool Softener
- Gentle, Dependable
- Relief in 6-12 Hours
TABLETS
**This product is not manufactured or distributed by Avrio Health L.P., distributor of Colace® 2-IN-1
TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING.
MADE WITH PRIDE AND CARE FOR H-E-B® SAN ANTONIO, TX 78204
- Product Label
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INGREDIENTS AND APPEARANCE
STOOL SOFTENER LAXATIVE
docusate sodium and sennosides tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37808-355 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DOCUSATE SODIUM (UNII: F05Q2T2JA0) (DOCUSATE - UNII:M7P27195AG) DOCUSATE SODIUM 50 mg SENNOSIDES (UNII: 3FYP5M0IJX) (SENNOSIDES - UNII:3FYP5M0IJX) SENNOSIDES 8.6 mg Inactive Ingredients Ingredient Name Strength CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP) FD&C RED NO. 40 (UNII: WZB9127XOA) HYPROMELLOSES (UNII: 3NXW29V3WO) MAGNESIUM STEARATE (UNII: 70097M6I30) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) TALC (UNII: 7SEV7J4R1U) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FD&C BLUE NO. 2 (UNII: L06K8R7DQK) Product Characteristics Color red Score no score Shape ROUND Size 10mm Flavor Imprint Code PSD21 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37808-355-24 240 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/30/2020 2 NDC:37808-355-12 120 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/30/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 06/30/2020 Labeler - H E B (007924756)