ONELAX SENNA- senna syrup

OneLAX SENNA by

Drug Labeling and Warnings

OneLAX SENNA by is a Otc medication manufactured, distributed, or labeled by Atlantic Biologicals Corp.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

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

Uses

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

Warnings

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

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

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,

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. Shake Well Before Using.

DOSAGE & ADMINISTRATION

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 yeart	l/2- 3/4teaspoon once a day	3/4 teaspoon twice a day
Children under 2 years	ask a doctor	ask a doctor

Other Information

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

Inactive Ingredients

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

KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental overdose, get medical help immediately or contact Poison Control Center immediately 1(800) 222-1222

To Report Adverse Drug Event contact the FDA at 1-800- FDA-1088 or www.fda.gov/medwatch.

Questions?

Call 1(800) 509-7592

Distributed By:

Atlaantic Biologicals Corp.

Miami, FL 33179

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ONELAX SENNA 
senna syrup

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 17856-8127(NDC:71399-0027)
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SENNOSIDES A AND B (UNII: 1B5FPI42EN) (SENNOSIDES A AND B - UNII:1B5FPI42EN)	SENNOSIDES A AND B	417.12 mg  in 237 mL

Inactive Ingredients
Ingredient Name	Strength
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
WATER (UNII: 059QF0KO0R)
SUCROSE (UNII: C151H8M554)

Product Characteristics
Color		Score
Shape		Size
Flavor	CHOCOLATE	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 17856-8127-2	50 in 1 CASE	10/10/2025
1		5 mL in 1 CUP, UNIT-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M007	02/06/2024

Labeler - Atlantic Biologicals Corp. (047437707)