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

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Laxacin

Alexso Inc

LaxacinLaxative Plus Stool Softener


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Docusate Sodium 50 mg

Sennosides 8.6 mg

Purpose

Stool Softener

Laxative

Laxacin Uses

  • relieves occasional constipation (irregularity)
  • generally produces a bowel movement in 6-12 hours

Warnings

Do not use

  • if you are now taking mineral oil, unless directed by a doctor
  • laxative products for longer than 1 week unless directed by a doctor

 

Ask a doctor before use if you have

  • stomach pain
  • nausea
  • vomiting
  • noticed a sudden change in bowel habits that continues over a period of 2 weeks

Stop use and ask a doctor if you have rectal bleeding or fail to have a bowel movement after use of a laxative.
These may indicate 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 right away.

LOT#

Exp. Date:

Directions

  • take preferably at bedtime or as directly by a doctor
age starting dose maximum dose
adults and children 12 years and older 2 tablets once a day 4 tablets twice a day

Other information

  • Each tablet contains: Calcium 20 mg
  • Each tablet contains: Sodium 4 mg
  • Store at room temperature
  • Keep lid tightly closed in a dry place
  • Do not use if imprinted safety seal under cap is broken or missing

Inactive ingredients

Croscarmellose Sodium, D&C Yellow #10, Dextrose, Dicalcium Phosphate, FD&C Yellow #6, Hypromelose, Magnesium Stearate, Microcrystalline Cellulose, Polyethylene Glycol, Silica, Sodium Benzoate, Stearic Acid, Titanium Dioxide.

Questions? If you have any questions or comments, or to report an adverse event, please contact (480) 253-9761.

Manufactured for:
Alexso Inc.
Thousand Oaks, CA 91360

Package/Label Principal Display Panel

Laxacin
Bottle Label

Laxacin

Docusate sodium and sennosides TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:50488-0901
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
DOCUSATE SODIUM DOCUSATE 50 mg
SENNOSIDES A AND B SENNOSIDES A AND B 8.6 mg

Inactive Ingredients

Ingredient Name Strength
CROSCARMELLOSE SODIUM
D&C YELLOW NO. 10
DEXTROSE
ANHYDROUS DIBASIC CALCIUM PHOSPHATE
FD&C YELLOW NO. 6
HYPROMELLOSES
MAGNESIUM STEARATE
cellulose, microcrystalline
POLYETHYLENE GLYCOLS
SODIUM BENZOATE
STEARIC ACID
titanium dioxide

Product Characteristics

Color Size Imprint Code Shape
ORANGE 10 mm G55 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:50488-0901-1 100 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part334 2011-10-01


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Be sure to consult your doctor before taking any medication!
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