Geri-kot

Manufacturer
Bryant Ranch Prepack
Effective date
2024-12-11
Label type
HUMAN OTC DRUG LABEL
Version
102
Source
legacy-cache
Hydrated at
2026-08-01 20:44:22

Label at a glance#

ProductGeri-kot
Active ingredientSENNOSIDES
Label structure9 sections

Indications and uses

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

Dosage and administration

• 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

Storage and handling

each tablet contains: calcium 30 mg Tamper Evident: Do not use if imprinted seal under cap is missing or broken store at 20°C-25°C (68°F-77°F)

Label contents#

Full prescribing information#

Active ingredient (in each tablet)

OTC - ACTIVE INGREDIENT SECTION

Sennosides 8.6 mg

Purpose

OTC - PURPOSE SECTION

Laxative

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS 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
• have noticed a sudden change in bowel habits that lasts over 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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• 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

STORAGE AND HANDLING SECTION

  • each tablet contains: calcium 30 mg
  • Tamper Evident: Do not use if imprinted seal under cap is missing or broken
  • store at 20°C-25°C (68°F-77°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

croscarmellose sodium, dicalcium phosphate, hypromellose, magnesium stearate, microcrystalline cellulose, silica, talc, triacetin

HOW SUPPLIED

How Supplied Section

Sennosides 8.6 mg

  • NDC: 71335-2230-1: 100 Tablets in a BOTTLE
  • NDC: 71335-2230-2: 60 Tablets in a BOTTLE
  • NDC: 71335-2230-3: 120 Tablets in a BOTTLE
  • NDC: 71335-2230-4: 56 Tablets in a BOTTLE
  • NDC: 71335-2230-5: 30 Tablets in a BOTTLE
  • NDC: 71335-2230-6: 90 Tablets in a BOTTLE
  • NDC: 71335-2230-7: 10 Tablets in a BOTTLE

Repackaged/Relabeled by:
Bryant Ranch Prepack, Inc.
Burbank, CA 91504

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sennosides 8.6 mg Tablets

LabelLabel

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
57896-415-01EA - Each57896-41535474003-2d89-4f7c-8b19-f04514fdecb312023-05-05
57896-415-10EA - Each57896-415c7308376-15ce-4e13-8ed0-5846bc0219d912023-04-07

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
fb8f8a8d-65ef-457b-9e18-81db646b55fd1c5791f9-950d-4e24-89e8-b7736e40444c2024-12-11WarningsExact identifier
spl id: fb8f8a8d-65ef-457b-9e18-81db646b55fd
spl set id: 1c5791f9-950d-4e24-89e8-b7736e40444c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.