ONELAX SALINE LAXATIVE- magnesium citrate liquid 
AKRON PHARMA INC

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OneLAX (Magnesium Citrate)
Sugar Free / Dye Free
Relief of occasional Constipation

Drug Facts

Active ingredient (30ml (approx. 1 Fl. oz))

Magnesium citrate 1.745g

Purpose

Saline laxative

Uses

Warnings

Do not use

 laxative products for longer than 1 week unless directed by a doctor.

Ask a doctor before use if you have

  • kidney disease
  • a magnesium restricted diet
  • a sodium restricted diet
  • stomach pain, nausea or vomiting
  • noticed a sudden change in bowel habits that lasts more than 1 week

Ask a doctor or pharmacist before use if you are

presently taking a prescription drug.

When using this product

do not exceed the maximum recommended daily dosage in a 24 hour period.

Stop use and ask a doctor if

you have rectal bleeding or no bowel movement after use. These could be signs of 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 (1-800-222-1222) right away.

Directions

 adults and children 12 years of age and over 1/2 bottle to 1 bottle (10 fl oz)
 children 6 to 11 years of age 1/3 bottle to 1/2 bottle
 children under 6 years of age consult a doctor

Other information

Inactive ingredients

citric acid, disodium edetate, cherry flavor, purified water, saccharin sodium, sodium benzoate, sorbic acid

Questions or comments?

Call  toll-free 1-877-225-6999.

Manufactured for:

Akron Pharma Inc.,

Fairfield, NJ-07004 

www.akronpharma.com

cherry

ONELAX  SALINE LAXATIVE
magnesium citrate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71399-0053
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MAGNESIUM CITRATE (UNII: RHO26O1T9V) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM CITRATE1.745 g  in 29.6 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
WATER (UNII: 059QF0KO0R)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SORBIC ACID (UNII: X045WJ989B)  
Product Characteristics
Color    Score    
ShapeSize
FlavorCHERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71399-0053-1296 mL in 1 BOTTLE; Type 0: Not a Combination Product02/06/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00702/06/2024
Labeler - AKRON PHARMA INC (067878881)

Revised: 2/2024
Document Id: 185d96ce-5a7a-445f-bc02-af9155955e87
Set id: e6de00e6-dd81-4aab-af23-04fab261c6ff
Version: 1
Effective Time: 20240210
 
AKRON PHARMA INC