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

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Lidocaine Hydrochloride

Safetec of America, Inc.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredients

Lidocaine HCl 2.0%

Purpose

Topical pain relief

Uses

Temporary pain relief for minor burns

Warnings

For external use only

Do not use

  • in large quantities, particularly over raw or blistered areas
  • near eyes, if this happens rinse thoroughly with water

Stop use and ask a doctor if condition worsens or persists for more than 7 days or clears up and returns

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

Directions

  • for adults and children 2 years of age and older: spray an even layer of burn spray over cleaned affected area not more than 3-4 times daily
  • for children under 2 years of age consult a physician

Inactive ingredients

aloe vera, germaben II, propylene glycol, purified water

Manufactured by SAFETEC OF AMERICA, Inc.

Buffalo, NY 14215 800-456-7077 www.safetec.com

PAIN RELIEF – Burn Spray 
Safetec of America

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
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PRINCIPAL DISPLAY PANEL – 3 oz. bottle

NDC 61010-5100-3

Safetec

First Aid
Burn Spray

For Temporary
Pain Relief of
Minor Burns

3 fl. oz. (88.7 ml)

Reorder no. 50104

Lidocaine Hydrochloride

Lidocaine Hydrochloride LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:61010-5100
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
LIDOCAINE HYDROCHLORIDE LIDOCAINE 20 mg

Inactive Ingredients

Ingredient Name Strength
Aloe Vera Leaf
propylene glycol
DIAZOLIDINYL UREA
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:61010-5100-3 88.7 in 1 BOTTLE, SPRAY

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2011-08-02


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Be sure to consult your doctor before taking any medication!
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