OneLAX SENNA SYRUP

Manufacturer
Akron Pharma Inc.
Effective date
2026-09-01
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
daily-update
Hydrated at
2026-09-03 03:03:52

Label at a glance#

ProductOneLAX SENNA
Active ingredientSENNOSIDES A AND B
Label structure9 sections

Indications and uses

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

Dosage and administration

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

Storage and handling

Avoid accessive heat. Store at room temperature 15°-30°C (59°-86°F)

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active ingredient(in each teaspoonful)          Purpose
Sennosides 8.8 mg …………………………................Laxative

Uses

OTC - PURPOSE SECTION

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

Warnings

WARNINGS 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

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

Ask a doctor or pharmacist before use if

OTC - ASK DOCTOR SECTION

you are taking any other drug. Take this product two more hours before or after other drugs. Laxatives may affect how other drugs work.

Stop use and ask a doctor if

OTC - STOP USE SECTION

you have rectal bleeding or fail to have bowel movement after use of laxative. This may indicate a serious condition.

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

INDICATIONS & USAGE SECTION

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

DOSAGE & ADMINISTRATION SECTION

 age starting dose maximum dosage
 Adults and children 12 yeart and older 2-3 teaspoons once a day 3 teaspoons twice a day
 Children 6 years to under 12 yeart 1 - 1 1/2teaspoons once a day  1 1/2teaspoons twice a day
 Children 2 years to under 6 yeartl/2- 3/4teaspoon once a day  3/4 teaspoon twice a day
 Children under 2 years ask a doctor ask a doctor

Other Information

STORAGE AND HANDLING SECTION

  • Avoid accessive heat. Store at room temperature 15°-30°C (59°-86°F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

flavor choclate, mythylparaben, propylene glycol, propylparaben, purified water and sucrose

KEEP OUT OF REACH OF CHILDREN SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental overdose, get medical help or contact a Poison Control Center immediately

Questions?

To Report Adverse Drug Event Call 1(877) 225-6999

Manufactured for:

Akron Pharma Inc.,

Fairfield, NJ-07004

package label principal display

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
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 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71399-002771399-0027-8

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

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22025-10-27full-release2026-06-01 01:40:56
12024-02-10full-release2026-06-01 00:08:29

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
OneLAX SENNASENNAAkron Pharma Inc.27fa8f54-ed84-4afd-8da3-8754da48643b2026-09-01WarningsExact identifier
ndc (package): 71399-0027-8
ndc (product): 71399-0027
ndc11 (package): 71399002708
spl id: 5a6593f8-d323-3cb0-e063-6294a90a0dba
spl set id: 27fa8f54-ed84-4afd-8da3-8754da48643b

Reported adverse events (FAERS/openFDA)#

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