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Microcaine Topical Analgesic

Medically reviewed on January 22, 2018

Dosage form: cream
Ingredients: LIDOCAINE 50mg in 1g
Labeler: Unit Dose, Ltd.
NDC Code: 67194-022

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.

Microcaine Topical Analgesic Cream

Drug Facts

Active Ingredient

Lidocaine 5% w/w

Purpose

Local Anesthetic

Uses:

Temporarily relieves pain from anorectal origin.

WARNINGS

For External Use only

When using this product
  • Do not get into the eyes
  • Do not use more than directed
  • Do not swallow

Stop use and ask a doctor if
  • pain worsens or does not improve within 7 days or clears up and appears again in a few days
  • ​you develop an allergy

Keep out of reach of children
  • If swallowed, get medical help right away or contact a Poison Control Center right away. NDC 67194-022-01

Directions:

​Children under 12 years-ask a doctor

  • Adults: Apply 1-2 gm to desired area and wait 12 to 60 minutes. Remove excess. May repeat 2-3 times/day.

Questions?

​Call toll free 888/452-4946

Inactive ingredients:

Water (Aqua), Prolatum Oil. Stearyl Alcohol, Polysorbate 60, Cetearyl Alcohol, Glyceryl Stearate, Carbomer, Triethanolamine, Propylparaben, Propylene Glycol, Methylparaben, Disodium EDTA, Diazolidinyl Carbamide, BHT

​Package Labeling:

MICROCAINE TOPICAL ANALGESIC 
lidocaine cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67194-022
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE (LIDOCAINE) LIDOCAINE50 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
WATER 
STEARYL ALCOHOL 
POLYSORBATE 60 
CETOSTEARYL ALCOHOL 
GLYCERYL MONOSTEARATE 
TROLAMINE 
PROPYLPARABEN 
PROPYLENE GLYCOL 
METHYLPARABEN 
EDETATE DISODIUM 
BUTYLATED HYDROXYTOLUENE 
Packaging
#Item CodePackage Description
1NDC:67194-022-0115 g in 1 JAR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34601/19/2016
Labeler - Unit Dose, Ltd. (119080393)
Establishment
NameAddressID/FEIOperations
Unit Dose, Ltd.119080393relabel(67194-022)

 
Unit Dose, Ltd.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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