Benzalkonium Chloride Towelette description, usages, side effects, indications, overdosage, supplying and lots more!

Benzalkonium Chloride Towelette

PSS World Medical, Inc.
Shanghai Yinjing Medical Supplies Co., Ltd.

  • Description
  • Clinical Pharmacology
  • Indications & Usage
  • Contraindications
  • Warnings
  • Precautions
  • Side Effects
  • Overdosage
  • Dosage & Administration
  • How Supplied
  • Patient Counseling Information
  • Supplemental Patient Material
  • Boxed Warning
  • Patient Package Insert
BENZALKONIUM CHLORIDE TOWELETTE (benzalkonium chloride) liquid[PSS World Medical]

FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Active ingredient                                

Benzalkonium Chloride, 0.13% w/v

Purpose

Purpose

First Aid Antiseptic

Uses

Use First aid antiseptic to help prevent the risk of infection in minor cuts, scrapes and burns.

Warnings

For external use only.


Do not use  

  • in the eyes or apply over large areas of the body.
  • longer than 1 week unless directed by a doctor.

Consult a doctor in case of deep or puncture wounds, animal bites, or serious burns.

Stop use and consult a doctor if the condition persists or gets worse.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Clean the affected area
  • Apply a small amount of this product on the area 1 to 3 times daily
  • May be covered with a sterile bandage when dry

Inactive ingredients purified water, sodium bicarbonate

Comments or Questions about Select Medical Products? 800-777-4908

Manufactured for PSS World Medical, Inc.

4345 Southpoint Blvd., Jacksonville, FL 32216

Made in China  www.myselectonline.com

Package Label

Reorder #269

NDC 68345-883-50

269_Each

Package Label

269_Box

Package Label

269_Case

Package Label

Benzalkonium Chloride Towelette

BENZALKONIUM CHLORIDE LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:68345-883
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
benzalkonium chloride 0.13 g

Inactive Ingredients

Ingredient Name Strength
water
SODIUM BICARBONATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 1.5 in 1 PACKET
2 100 in 1 BOX
3 NDC:68345-883-50 10 in 1 CASE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partE part333E 2013-06-20


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Be sure to consult your doctor before taking any medication!
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