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

Menu
Search

Lidocaine

PD-Rx Pharmaceuticals, Inc.
PD-Rx Pharmaceuticals, Inc.

Lidocaine 4%


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredient


Lidocaine 4% w/w

Purpose

Topical anesthetic

Use

temporarily relieves pain and itching due to

  • minor cuts
  • minor scrapes
  • minor burns
  • sunburn
  • minor skin irritations
  • minor bites

WARNINGS:

For external use only

When using this product

Do not use

  • in or near the eyes
  • in large quantities, particularly over raw surfaces or blistered areas

Stop use

Stop use and ask doctor if:

  • allergic reaction occurs
  • condition worsens or does not improve within 7 days
  • symptoms clear up and return within a few days
  • redness, irritation, swelling, pain or other symptoms begin or increase
Keep out of the reach of children

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

Directions

  • Adults and children 2 years and older: Apply externally to the affected area up to 3 to 4 times a day.
  • Children under 2 years of age: Consult a doctor

Other Information

  • May be applied under occlusive dressing
  • Store at 25 deg. C (77F); excursions permitted to 15-30 deg. C (59-86F)
  • [see USP Controlled Room Temperature].

Inactive ingredients

water, cetyl alcohol, stearic acid, aloe barbadensis leaf juice, simmondsia chinensis (jojoba) seed oil,

lecithin, hexylene glycol, sodium polyacrylate, caprylyl glycol, ethoxydiglycol, potassium sorbate, phenoxyethanol

Lidocaine 4%

Lidocaine

Lidocaine

Lidocaine CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:68752-024
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
LIDOCAINE LIDOCAINE 4 g

Inactive Ingredients

Ingredient Name Strength
water
CETYL ALCOHOL
STEARIC ACID
Aloe Vera Leaf
Jojoba Oil
Hexylene Glycol
CAPRYLYL GLYCOL
DIETHYLENE GLYCOL MONOETHYL ETHER
POTASSIUM SORBATE
PHENOXYETHANOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 45 in 1 TUBE
2 NDC:68752-024-05 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2011-10-01


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.