Onelax Senna Senna Syrup

Manufacturer
Precision Dose, Inc.
Effective date
2024-07-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:15:36

Label at a glance#

ProductSENNA
Active ingredientSennosides A and B
Label structure13 sections

Indications and uses

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

Dosage and administration

take preferably at bedtime or as directed by a doctor. Shake Well Before Using. age starting dose maximum dosage Adults and children 12 years and older 2-3 teaspoons once a day 3 teaspoons twice a day Children 6 years to under 12 years 1-1½ teaspoons once a day 1½ teaspoons twice a day Children 2 years to under 6 years ½ - ¾ teaspoon once a day ¾ teaspoon twice a day Children under 2 years ask a doctor ask a doctor

Storage and handling

avoid excessive heat store at room temperature 15°-30°C (59°-86°F)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Senna Syrup
Natural Chocolate Flavor
8.8 mg/5 mL

For Hospital Use Only

Drug Facts

Active ingredient (in each teaspoonful)

OTC - ACTIVE INGREDIENT SECTION

Sennosides 8.8 mg

Purpose

OTC - PURPOSE SECTION

Laxative

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

OTC - ASK DOCTOR SECTION

ask a doctor before use if you have

  • stomach pain
  • nausea
  • vomiting
  • noticed a sudden change in bowel movements that continues over a period of 2 weeks

OTC - DO NOT USE SECTION

Do not use laxative products for longer than 1 week unless directed by a doctor

OTC - ASK DOCTOR/PHARMACIST SECTION

Ask a doctor or pharmacist before use if you are taking any other drug. Take this product two or more hours before or after other drugs. Laxatives may affect how other drugs work.

OTC - STOP USE SECTION

Stop use and ask a doctor if you have rectal bleeding or fail to have bowel movement after use of laxative.

These may indicate a serious condition.

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

take preferably at bedtime or as directed by a doctor. Shake Well Before Using.

agestarting dosemaximum dosage
Adults and children 12 years and older2-3 teaspoons once a day3 teaspoons twice a day
Children 6 years to under 12 years1-1½ teaspoons once a day1½ teaspoons twice a day
Children 2 years to under 6 years½ - ¾ teaspoon once a day¾ teaspoon twice a day
Children under 2 yearsask a doctorask a doctor

Other information

STORAGE AND HANDLING SECTION

  • avoid excessive heat
  • store at room temperature 15°-30°C (59°-86°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

flavor chocolate, methylparaben, propylene glycol, propylparaben, purified water and sucrose.

Questions or comments?

OTC - QUESTIONS SECTION

To Report Adverse Drug Events Call (815) 397-9228

SPL UNCLASSIFIED SECTION

Alcohol Free, Gluten Free, Natural Vegetable Laxative

How Supplied

HOW SUPPLIED SECTION

NDC 68094-049-62
5 mL per unit dose cup
Thirty (30) cups per shipper

SPL UNCLASSIFIED SECTION

Manufactured for:
Akron Pharma Inc.
Fairfield, NJ 07004

Packaged by:
Precision Dose, Inc.
South Beloit, IL 61080

For inquiries call Precision Dose, Inc. at 1-800-397-9228 or email druginfo@precisiondose.com

LI1378 Rev. 09/21

PRINCIPAL DISPLAY PANEL - 5 mL Cup Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 68094-049-59
PrecisionDose™

Senna Syrup
8.8 mg/5 mL

Pkg: Precision Dose, Inc., S. Beloit, IL 61080

PRINCIPAL DISPLAY PANEL - 5 mL Cup Label
PRINCIPAL DISPLAY PANEL - 5 mL Cup Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
702311sennosides 8.8 MG in 5 mL Oral SolutionPSN2
702311sennosides, USP 1.76 MG/ML Oral SolutionSCD2
702311sennosides 8.8 MG per 5 mL Oral SyrupSY2
702311sennosides, USP 26.4 MG per 15 ML Oral SolutionSY2
702311sennosides, USP 8.8 MG per 5 ML Oral SolutionSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68094-049-59SENNA5 mL in 1 CUP, UNIT-DOSESYRUP52
68094-049-62SENNA10 in 1 TRAYSYRUP102
68094-049-62SENNA3 in 1 CASESYRUP32

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68094-049SENNA SYRUP [PRECISION DOSE, INC.]2Current NDC, 3 package rows20240719_e637777e-a39d-4e2f-a95c-4f524aa122f7.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68094-049-59ML - Milliliter68094-0499dbeca0f-1691-42f6-b5fc-481082a6764912024-07-12
68094-049-62ML - Milliliter68094-049be2c8753-1fd8-4128-bf2f-ce768e81088b12024-07-12
71399-0027-8ML - Milliliter71399-0027fe9b506a-3920-4704-9b2c-1015086984ee12024-03-12

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68094-04968094-049-59, 68094-049-62
71399-0027

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
OneLAX SENNASENNAAkron Pharma Inc.27fa8f54-ed84-4afd-8da3-8754da48643b2026-09-01WarningsExact identifier
ndc (product): 71399-0027
SENNASENNAPrecision Dose, Inc.e637777e-a39d-4e2f-a95c-4f524aa122f72024-07-05WarningsExact identifier
ndc (package): 68094-049-59
ndc (package): 68094-049-62
ndc (product): 68094-049
ndc11 (package): 68094004959
ndc11 (package): 68094004962
spl id: e6e1ea89-0223-4a05-915a-77ec0d923815
spl set id: e637777e-a39d-4e2f-a95c-4f524aa122f7

Reported adverse events (FAERS/openFDA)#

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