DOCUSATE CALCIUM 240 MG SODIUM FREE- docusate calcium capsule, liquid filled 
AvPAK

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Docusate Calcium

Active ingredient

Docusate Calcium 240 mg

Purpose

Stool Softener

Uses

Warnings: Do not use

Ask a Doctor Before Use

if you notice a sudden change in bowel habits that persists over a period of two weeks.

Stop Use and Ask a Doctor If

If Pregnant or Breast Feeding

Ask a healthcare professional before use.

Keep Out of Reach of Children.

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

Directions

Adults and Children over 12 years of age

Take orally 1 softgel daily for 2 to 3 days or until bowl movements are normal, or as directed by a doctor.

Children under 12 years of age

Do not use this product for children under 12 years of age, unless directed by a doctor.

Other Information

Inactive Ingredients

Corn Oil, FD&C Blue #1, FD&C Red #40, Gelatin, Glycerin, Ink (Edible), Sorbitol Special.

Questions or Comments

Call 1-855-361-3993                 

Package/Label Principal Display Panel

NDC 50268-266-15

AvKARE                    

DOCUSATE
CALCIUM
SODIUM-FREE
STOOL SOFTENER
240 mg Each
100 Softgels

USA
AV Rev. 05/16 (P)          

Manufactured for:
AvKARE, Inc.
Pulaski, TN 38478

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DOCUSATE CALCIUM 240 MG SODIUM FREE 
docusate calcium capsule, liquid filled
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50268-266(NDC:54629-640)
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DOCUSATE CALCIUM (UNII: 6K7YS503HC) (DOCUSATE - UNII:M7P27195AG) DOCUSATE CALCIUM240 mg
Inactive Ingredients
Ingredient NameStrength
CORN OIL (UNII: 8470G57WFM)  
GELATIN (UNII: 2G86QN327L)  
GLYCERIN (UNII: PDC6A3C0OX)  
SORBITOL (UNII: 506T60A25R)  
WATER (UNII: 059QF0KO0R)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
Product Characteristics
ColorredScoreno score
ShapeOVALSize15mm
FlavorImprint Code NV02
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50268-266-1550 in 1 BOX05/17/2017
1NDC:50268-266-111 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00705/17/2017
Labeler - AvPAK (832926666)

Revised: 10/2023
Document Id: 09060222-ce98-8e02-e063-6294a90af117
Set id: 30ea2e6f-62f4-462e-ad70-5ec77cb82ae5
Version: 7
Effective Time: 20231031
 
AvPAK