DOK description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

DOK

Cardinal Health

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Drug Facts

Active Ingredient (in each softgel)

Docusate Sodium, USP, 100 mg

Purpose

Stool Softener

Keep Out of Reach of Children

Keep out of reach of children.

DOK Uses

For prevention of dry, hard stools, for relief of occasional constipation. This product generally produces a bowel movement within 12 to 72 hours.

Warnings

This package is intended for institutional use only. In case of overdose, get medical help or contact a Poison Control Center right away.

Do not use if you are currently taking mineral oil, unless directed by a doctor, when abdominal pain, nausea, or vomiting are present, for longer than one week unless directed by a doctor.

Ask a doctor before use if you notice a sudden change in bowel habits that persists over a period of 2 weeks. Stop use and ask a doctor if you have rectal bleeding or if you fail to have a bowel movement after use.

If pregnant or breast-feeding ask a health professional before use.

Directions

Adults and children over 12 years of age, take 2 softgels, preferably at bedtime

children 6 to 12 years of age take 1 softgel at bedtime

Inactive ingredients

FD&C red #40, FD&C yellow #6, gelatin, glycerin, polyethylene glycol, propylene glycol, purified water and sorbitol special

Storage

Store at 20 - 25 C (68 - 77 F); excursions permitted to 15 - 30 C (59-86 F). [See USP Controlled Room Temperature]

Other Information

Each softgel contains: sodium 5 mg

For use as a Stool Softener in Treating & Avoiding Constipation

Distributed by

Major Pharmaceuticals

31778 Enterprise Drive

Livonia, MI 48150 USA

MFGD By Banner Pharmacaps, Inc., NC 27265

Questions? Adverse Drug Event

Call (800) 616-2471

DOK 100 mg

Docusate Sodium Softgels, USP

10 Softgel Capsules

Repackaged by Cardinal Health

Zanesville, OH 43701

L34321501012

Package/Label Principal Display Panel

DOK 100 MG.

Docusate Sodium Softgels, USP

10 Softgel Capsules

DOK

DOK

Docusate Sodium CAPSULE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:55154-0667(NDC:0904-2244)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
DOCUSATE SODIUM DOCUSATE 100 mg

Inactive Ingredients

Ingredient Name Strength
FD&C RED NO. 40
FD&C YELLOW NO. 6
GELATIN
GLYCERIN
POLYETHYLENE GLYCOL 3350
propylene glycol
water
sorbitol

Product Characteristics

Color Size Imprint Code Shape
ORANGE 13 mm P51 CAPSULE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 1 in 1 BLISTER PACK
2 NDC:55154-0667-0 10 in 1 BAG

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2011-06-06


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.