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NDC 61919-0684-60 SENNA PLUS 50; 8.6 mg/1; mg/1 Details
SENNA PLUS 50; 8.6 mg/1; mg/1
SENNA PLUS is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by DIRECTRX. The primary component is DOCUSATE SODIUM; SENNOSIDES.
MedlinePlus Drug Summary
Senna is used on a short-term basis to treat constipation. It also is used to empty the bowels before surgery and certain medical procedures. Senna is in a class of medications called stimulant laxatives. It works by increasing activity of the intestines to cause a bowel movement.
Related Packages: 61919-0684-60Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Senna
Stool softeners are used on a short-term basis to relieve constipation by people who should avoid straining during bowel movements because of heart conditions, hemorrhoids, and other problems. They work by softening stools to make them easier to pass.
Related Packages: 61919-0684-60Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Stool Softeners
Product Information
NDC | 61919-0684 |
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Product ID | 61919-684_835c6547-8bdd-6455-e053-2991aa0a0d78 |
Associated GPIs | |
GCN Sequence Number | n/a |
GCN Sequence Number Description | n/a |
HIC3 | n/a |
HIC3 Description | n/a |
GCN | n/a |
HICL Sequence Number | n/a |
HICL Sequence Number Description | n/a |
Brand/Generic | n/a |
Proprietary Name | SENNA PLUS |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | SENNA PLUS |
Product Type | HUMAN OTC DRUG |
Dosage Form | TABLET |
Route | ORAL |
Active Ingredient Strength | 50; 8.6 |
Active Ingredient Units | mg/1; mg/1 |
Substance Name | DOCUSATE SODIUM; SENNOSIDES |
Labeler Name | DIRECTRX |
Pharmaceutical Class | n/a |
DEA Schedule | n/a |
Marketing Category | OTC MONOGRAPH NOT FINAL |
Application Number | part334 |
Listing Certified Through | 2023-12-31 |
Package
Package Images

NDC 61919-0684-60 (61919068460)
NDC Package Code | 61919-684-60 |
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Billing NDC | 61919068460 |
Package | 60 TABLET in 1 BOTTLE (61919-684-60) |
Marketing Start Date | 2019-03-06 |
NDC Exclude Flag | N |
Pricing Information | N/A |
Standard Product Labeling (SPL)/Prescribing Information SPL 830d195a-d5d5-b3e5-e053-2991aa0aee2a Details
SPL UNCLASSIFIED SECTION
SPL UNCLASSIFIED SECTION
Do not use for more than 1 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 2 weeks
Stop use and ask a doctor if -you have no bowel movement within 12 hours -you have rectal bleeding. these could signs of 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.
INSTRUCTIONS FOR USE
SPL UNCLASSIFIED SECTION
SPL UNCLASSIFIED SECTION
SPL UNCLASSIFIED SECTION
INGREDIENTS AND APPEARANCE
SENNA PLUS
senna plus tablet |
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Labeler - DIRECTRX (079254320) |
Registrant - DIRECTRX (079254320) |
Establishment | |||
Name | Address | ID/FEI | Business Operations |
---|---|---|---|
DIRECTRX | 079254320 | repack(61919-684) |