Label: CVS HEALTH SENNA PLUS STOOL SOFTENER LAXATIVE SOFTGEL- docusate sodium, sennosides capsule, liquid filled
- NDC Code(s): 51316-902-06
- Packager: CVS Pharmacy, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 17, 2024
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredients (in each softgel)
- Purpose
- Uses
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Warnings
Do not use • if you are now taking mineral oil, unless directed by a doctor • laxative products for longer than 1 week unless directed by a doctor
Ask a doctor before use if you have • stomach pain • nausea • vomiting • noticed a sudden change in bowel habits that continues over a period of 2 weeks
Stop use and ask a doctor if you have rectal bleeding or fail to have a bowel movement after use of a laxative. These may indicate a serious condition.
If pregnant or breast-feeding, ask a health professional before use.
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Directions
• take preferably at bedtime or as directed by a doctor
Age Starting Dosage Maximum Dosage adults and children 12 years of age and over 2 softgels once a day 4 softgels twice a day children 6 to under 12 years 1 softgel once a day 2 softgels twice a day children under 6 years of age ask a doctor ask a doctor - Other information
- Inactive ingredients
- Questions?
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SPL UNCLASSIFIED SECTION
Compare to the active ingredients in Senokot-S®*
Liquid Filled Softgels
Natural vegetable laxative ingredient plus stool softener
Actual Product Size on Bottom Panel
*This product is not manufactured or distributed by Avrio Health L.P., owner of the registered trademark Senokot-S®*.
Package Contains One Bottle
Overnight, gentle laxative
Distributed by: CVS Pharmacy, Inc.
One CVS Drive, Woonsocket, RI 02895
@2024 CVS/pharmacy
CVS.com® 1-800-SHOP CVSProduct of India
TAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING
READ AND KEEP OUTER CARTON FOR COMPLETE PRODUCT WARNINGS AND INFORMATION
- Packaging
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INGREDIENTS AND APPEARANCE
CVS HEALTH SENNA PLUS STOOL SOFTENER LAXATIVE SOFTGEL
docusate sodium, sennosides capsule, liquid filledProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51316-902 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 SILICON DIOXIDE (UNII: ETJ7Z6XBU4) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) GELATIN, UNSPECIFIED (UNII: 2G86QN327L) GLYCERIN (UNII: PDC6A3C0OX) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SORBITOL (UNII: 506T60A25R) SORBITAN (UNII: 6O92ICV9RU) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) YELLOW WAX (UNII: 2ZA36H0S2V) Product Characteristics Color orange Score no score Shape OVAL Size 12mm Flavor Imprint Code 902 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51316-902-06 1 in 1 CARTON 01/17/2024 1 60 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 Drug M007 01/17/2024 Labeler - CVS Pharmacy, Inc. (062312574)
