Pedia-Lax description, usages, side effects, indications, overdosage, supplying and lots more!

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Pedia-Lax

C.B. Fleet Company, Inc.

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredient (in each 59-mL delivered dose)

Monobasic Sodium Phosphate 9.5 g.................Saline Laxative

Use

For relief of occasional constipation.

Warnings

For rectal use only.



Ask a doctor before using this product if the child

  • is on a sodium-restricted diet
  • has kidney disease

Ask a doctor before using any laxative if the child has
  • abdominal pain, nausea, or vomiting
  • a sudden change in bowel habits lasting more than 2 weeks
  • already used a laxative for more than 1 week 

Stop use and consult a doctor if the child has

  • rectal bleeding
  • no bowel movement within 30 minutes of enema use
  • symptoms of dehydration (feeling thirsty, dizziness, vomiting or urinating less often than normal)

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Single Daily Dosage




children 5 to 11 years
1 bottle or as directed by a doctor
children 2 to under 5 years
one-half bottle (see below)
children under 2 years
DO NOT USE
One-half bottle prepararation:

Other Information

  • each 59-mL delivered dose contains: sodium 2.2 g
  • additional liquids by mouth are recommended while taking this product
  • this product generally produces a bowel movement in 1-5 minutes
  • carton sealed for safety. If seal with Fleet emblem on top or bottom flap is broken or missing, do not use
  • for complete professional use warnings and precautions, consult Physicians' Desk Reference

Inactive Ingredients

benzalkonium chloride, disodium EDTA, purified water

Questions?

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

Pedia-Lax

Pedia-Lax

sodium phosphate, dibasic and sodium phosphate, monobasic ENEMA

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0132-0202
Route of Administration RECTAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE SODIUM CATION 3.5 g
sodium phosphate, monobasic 9.5 g

Inactive Ingredients

Ingredient Name Strength
EDETATE DISODIUM
water
benzalkonium chloride

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0132-0202-20 66 in 1 BOTTLE, WITH APPLICATOR

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part334 2002-05-10


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Be sure to consult your doctor before taking any medication!
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