Search by Drug Name or NDC

NDC 79903-0045-12 Vegetable Laxative 8.6 mg/1 Details

Vegetable Laxative 8.6 mg/1

Vegetable Laxative is a ORAL TABLET, FILM COATED in the HUMAN OTC DRUG category. It is labeled and distributed by WALMART INC.. The primary component is 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: 79903-0045-12
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Senna

Product Information

NDC	79903-0045
Product ID	79903-045_9acb1a42-e3e5-4254-9bd6-9bb03ba0fa1d
Associated GPIs	46200060200303
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	Vegetable Laxative
Proprietary Name Suffix	n/a
Non-Proprietary Name	Sennosides
Product Type	HUMAN OTC DRUG
Dosage Form	TABLET, FILM COATED
Route	ORAL
Active Ingredient Strength	8.6
Active Ingredient Units	mg/1
Substance Name	SENNOSIDES
Labeler Name	WALMART INC.
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH NOT FINAL
Application Number	part334
Listing Certified Through	n/a

Package

Package Images

NDC 79903-0045-12 (79903004512)

Pricing Information	N/A
NDC Package Code	79903-045-12
Billing NDC	79903004512
Package	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-045-12)
Marketing Start Date	2021-02-15
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 1d500602-880b-427a-9977-58df68103dd9 Details

Active ingredient (in each tablet)

Sennosides USP, 8.6 mg

Purpose

Stimulant laxative

Uses

relieves occasional constipation (irregularity)
generally produces a bowel movement in 6 to 12 hours

Warnings

Do not use

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

When using this product

do not exceed recommended dosage.

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

take preferably at bedtime or as directed by a doctor

age	starting dosage	maximum dosage
adults and children 12 years and over	2 tablets once a day	4 tablets twice a day
children 6 to under 12 years	1 tablet once a day	2 tablets twice a day
children 2 to under 6 years	1/2 tablet once a day	1 tablet twice a day
children under 2 years	ask a doctor	ask a doctor

Other information

each tablet contains: calcium 30 mg, sodium 1 mg Very Low Sodium
store at 25°C (77°F); excursions permitted between 15°-30°C (59°-86°F)
protect from moisture
use by expiration date on package

Inactive ingredients

croscarmellose sodium, dibasic calcium phosphate dihydrate, hypromellose, magnesium stearate, maltodextrin, microcrystalline cellulose, polyethylene glycol, silicon dioxide

Questions or comments?

1-888-287-1915

Principal display panel

equate™

NDC 79903-045-12

Compare

to Senokot®

active

ingredient*

Vegetable

Laxative

Sennosides USP, 8.6 mg

Stimulant Laxative

• Gentle, overnight relief

• Vegetable laxative ingredient

8.6

mg

EACH

100

TABLETS

TAMPER EVIDENT: DO NOT USE IF

IMPRINTED SAFETY SEAL UNDER

CAP IS BROKEN OR MISSING

DISTRIBUTED BY: Walmart Inc., Bentonville, AR 72716

PRODUCT OF INDIA

*This product is not manufactured or distributed by

Avrio Health L.P., owner of the registered

trademark Senokot®. 50844 ORG102029812

Equate 44-298

INGREDIENTS AND APPEARANCE

VEGETABLE LAXATIVE

sennosides tablet, film coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:79903-045
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SENNOSIDES (UNII: 3FYP5M0IJX) (SENNOSIDES - UNII:3FYP5M0IJX)	SENNOSIDES	8.6 mg

Ingredient Name	Strength
Inactive Ingredients
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)

Product Characteristics
Color	brown	Score	no score
Shape	ROUND	Size	9mm
Flavor		Imprint Code	44;298
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:79903-045-12	100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/15/2021	04/28/2023

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part334	02/15/2021	04/28/2023

Labeler - WALMART INC. (051957769)

Name	Address	ID/FEI	Business Operations
Establishment
LNK International, Inc.		038154464	pack(79903-045)

Name	Address	ID/FEI	Business Operations
Establishment
LNK International, Inc.		832867894	manufacture(79903-045)

Name	Address	ID/FEI	Business Operations
Establishment
LNK International, Inc.		868734088	pack(79903-045)

Name	Address	ID/FEI	Business Operations
Establishment
LNK International, Inc.		967626305	pack(79903-045)

Revised: 12/2021

Document Id: 9acb1a42-e3e5-4254-9bd6-9bb03ba0fa1d

Set id: 1d500602-880b-427a-9977-58df68103dd9

Version: 2

Effective Time: 20211208