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Docuprene

Preferred Pharmaceuticals, Inc

DOCUPRENE 100mg (Sodium Dioctyl Sulfosuccinate)


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENT (in each tablet)


Sodium Dioctyl Sulfosuccinate          100mg       

Each tablet contains 8 mg. of Sodium

INACTIVE INGREDIENTS:

Dicalcium phosphate, microcrystalline cellulose, pregelatinized starch, croscamellose sodium, stearic acid, colloidal silicon dioxide, magnesium sterate, titanium dioxide, talc, hypromellose, polyethylene glycol, FDandC blue #1

PURPOSE


Stool softener



USES:


For the prevention of dry hard stools

For relief of occasional constipation

This product generally produces bowel movement with 12 to 72 hours.


WARNINGS:

Warnings

Do not use laxative products for longer that one week unless directed to do so by a doctor and if you are presently taking mineral oil, unless told to do so by a doctor.

Ask a doctor before use if you have: Abdominal pain, nausea, vomiting, noticed 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. These could be signs of a serious condition.

If pregnant or breast-feeding , ask a doctor before use.

OTHER INFORMATION

Other Information  

Store at room temperature 68- 77 degrees F

For Questions or Comments

Please email: info pnarx.com

or Call: 877-329-2592

KEEP OUT OF REACH OF CHILDREN

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

Adults and children 12 years of age and older: Take 1 or 2 tablets daily

Children Under 12 years of age: Do not use, Consult a doctor before use.

Bottle of 60 - 68788-9857-6

DOCUPRENE

100 mg

Sodium Dioctyl Sulfosuccinate

60 Tablets

Made in USA

Patent Pending

Manufactured For

Pharmaceutica  North America Glendale CA

Docuprene

Docuprene

DOCUSATE SODIUM TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:68788-9857(NDC:45861-201)
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
CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS
cellulose, microcrystalline
CROSCARMELLOSE SODIUM
STEARIC ACID
SILICON DIOXIDE
MAGNESIUM STEARATE
titanium dioxide
talc
HYPROMELLOSES
POLYETHYLENE GLYCOLS
FD&C BLUE NO. 1

Product Characteristics

Color Size Imprint Code Shape
blue (Blue) 11 mm C21 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:68788-9857-6 60 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part334 2012-03-12


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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