PEDIA-LAX- docusate sodium liquid 
C.B. Fleet Company, Inc.

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Pedia-lax Docusate Sodium Liquid 0132-0107

Drug Facts

Active Ingredients

(in each 15 mL)

Docusate Sodium 50 mg

Purpose

Stool softener

Uses

Warnings

Drug Interaction Precaution: Do not give this product to your child if your child is presently taking mineral oil, unless directed by a doctor.

Ask a doctor before using any laxative if your child has

  • a sudden change in bowel habits lasting more than 2 weeks
  • already used a laxative for more than 1 week

If constipation continues after 1 week of use, contact your child's doctor

Stop using this product and consult a doctor if your child has

  • rectal bleeding
  • no bowel movement within 72 hours of using this product

These symptoms may be signs of a serious condition.

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

 Age Dose
 Children 2 to under 12 years15 mL to 45 mL; do not take more than 45 mL in 24 hours
 Children under 2 years ask a doctor

Doses can be diluted in a suitable beverage to prevent throat irritation and to help mask the naturally tart flavor of the active ingredient (see side panel for info).

Other information

Inactive Ingredients

citric acid, edetate disodium, flavor, methylparaben, polyethylene glycol, povidone, propylene glycol, propylparaben, sodium citrate, sorbitol, sucralose, water, xanthan gum, xylitol

Questions?

1-866-255-6960 or www.pedia-lax.com

PRINCIPAL DISPLAY PANEL

Pedia-Lax
Docusate sodium
Liquid Stool Softener
4 fl oz (118 mL)

Pedia-Lax
Docusate sodium 
Liquid Stool Softener
4 fl oz (118 mL)

PEDIA-LAX 
docusate sodium liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0132-0107
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DOCUSATE SODIUM (UNII: F05Q2T2JA0) (DOCUSATE - UNII:M7P27195AG) DOCUSATE SODIUM50 mg  in 15 mL
Inactive Ingredients
Ingredient NameStrength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
POVIDONE (UNII: FZ989GH94E)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
SORBITOL (UNII: 506T60A25R)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
WATER (UNII: 059QF0KO0R)  
XANTHAN GUM (UNII: TTV12P4NEE)  
XYLITOL (UNII: VCQ006KQ1E)  
Product Characteristics
Colorwhite (Colorless) Score    
ShapeSize
FlavorBERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0132-0107-24118 mL in 1 CARTON; Type 0: Not a Combination Product02/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00702/01/2020
Labeler - C.B. Fleet Company, Inc. (003119054)

Revised: 5/2024
Document Id: 89a8b6ff-526d-4565-b4dd-1119ffebd8c7
Set id: 41f10fa8-2dd2-4fc5-ad29-b4f7a63ab3cb
Version: 2
Effective Time: 20240516
 
C.B. Fleet Company, Inc.