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- NDC Code(s): 57896-555-01, 57896-555-06, 57896-555-10, 57896-555-20
- Packager: Geri-Care Pharmaceutical Corp
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 30, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
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- Active ingredient (in each tablet)
- Purpose
Stool softener
Laxative
- Uses
- relieves occasional constipation (irregularity)
- this product generally produces a bowel movement in 6 to 12 hours
- Warnings
Do not use for more than one week unless directed by a doctor
Ask a doctor before use if you
- have abdominal pain, nausea or vomiting
- are taking mineral oil
- have noticed a sudden change in bowel habits that lasts over two 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.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
- Directions
• do not exceed 8 tablets in 24 hours
Age Starting Dose Maximum Dose adults and children 12 years of age and older 2 tablets once a day preferably at bedtime; increase as needed, or as directed by a doctor 4 tablets in the morning and 4 tablets at bedtime children under 12 years ask a doctor - Other information
- each tablet contains: calcium 20 mg, sodium 3 mg
- store at controlled room temperature
Tamper Evident: Do not use if imprinted seal under cap is missing or broken. - product of India
- Inactive ingredients
cellulose, croscarmellose sodium, dicalcium phosphate, FD&C yellow #6 lake, hypromellose, magnesium stearate, PEG, silica, talc, titanium dioxide.
- Package Label
- INGREDIENTS AND APPEARANCE
SENNA-PLUS
sennosides and docusate sodium tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:57896-555 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SENNOSIDES (UNII: 3FYP5M0IJX) (SENNOSIDES - UNII:3FYP5M0IJX) SENNOSIDES 8.6mg DOCUSATE SODIUM (UNII: F05Q2T2JA0) (DOCUSATE - UNII:M7P27195AG) DOCUSATE SODIUM 50mg Inactive Ingredients Ingredient Name Strength CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: L11K75P92J) MAGNESIUM STEARATE (UNII: 70097M6I30) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) HYPROMELLOSES (UNII: 3NXW29V3WO) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) TALC (UNII: 7SEV7J4R1U) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) Product Characteristics Color orange Score no score Shape ROUND Size 9mm Flavor Imprint Code PSD22 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:57896-555-01 100 in 1 BOTTLE; Type 0: Not a Combination Product 05/01/2019 2 NDC:57896-555-06 60 in 1 BOTTLE; Type 0: Not a Combination Product 05/01/2019 3 NDC:57896-555-10 1000 in 1 BOTTLE; Type 0: Not a Combination Product 05/01/2019 4 NDC:57896-555-20 200 in 1 BOTTLE; Type 0: Not a Combination Product 05/01/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 05/01/2019 Labeler -Geri-Care Pharmaceutical Corp(611196254)
Registrant -Geri-Care Pharmaceutical Corp (611196254)
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Safety
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Related Resources
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More Info on this Drug
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View Labeling Archives for this drug
SENNA-PLUS- sennosides and docusate sodium tablet
Number of versions: 5
| Published Date (What is this?) | Version | Files |
|---|---|---|
| Dec 1, 2023 | 5 (current) | download |
| Oct 24, 2023 | 4 | download |
| Nov 16, 2022 | 3 | download |
| Sep 9, 2020 | 2 | download |
| May 30, 2019 | 1 | download |
RxNorm
SENNA-PLUS- sennosides and docusate sodium tablet
| RxCUI | RxNorm NAME | RxTTY | |
|---|---|---|---|
| 1 | 998740 | sennosides 8.6 MG / docusate sodium 50 MG Oral Tablet | PSN |
| 2 | 998740 | docusate sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet | SCD |
| 3 | 998740 | DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet | SY |
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SENNA-PLUS- sennosides and docusate sodium tablet
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NDC Codes
SENNA-PLUS- sennosides and docusate sodium tablet
If this SPL contains inactivated NDCs listed by the FDA initiated compliance action, they will be specified as such.
| NDC | |
|---|---|
| 1 | 57896-555-01 |
| 2 | 57896-555-06 |
| 3 | 57896-555-10 |
| 4 | 57896-555-20 |
