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Numquick Topical Analgesic

Medically reviewed by Drugs.com. Last updated on Dec 11, 2020.

Dosage form: gel
Ingredients: EPINEPHRINE HYDROCHLORIDE 0.1mg in 1mL, LIDOCAINE HYDROCHLORIDE 50mg in 1mL
Labeler: Unit Dose, Ltd.
NDC Code: 67194-005

Numquick Topical Analgesic

Drug Facts

Active ingredient

(-) Epinephrine HCL w/w 0.01%

Lidocaine HCl 5% w/w

Purpose

Vasoconstrictor

Local Anesthetic

Uses:

Temporarily relieves local discomfort or pain or burning associated with anorectal disorders.

Warnings:

​External use only

Allergy alert: ​certain persons can develop allergic reactions to the ingredients in this product.

Do not use:

this product in the rectum by using fingers or any mechnical device or applicator.

When using this product

do not use more than directed.

Stop use and ask a doctor

if pain worsens or does notimprove in 7 days

  • if redness, irritation, swelling, pain or other symptoms develop or increase
  • if bleeding occurs

Keep out of reach of children.

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

Directions:
  • adults: clean the affected area with mild soap and warm water and rinse thoroughly
  • dry gently
  • apply 1-2 g. externally to the affected area up to 4 times daily
  • children under 12 years: ask a doctor.

Other information:

Store in a cool dark place

Inactive ingredients:

Aqua (DI water), chlorobutanol, methylcellulose, sodium EDTA, sodium metabisulfite

Questions?

Call Toll Free 888-452-4946

Package Labeling:

NUMQUICK TOPICAL ANALGESIC 
epinephrine hydrochloride, lidocaine hydrochloride gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67194-005
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
EPINEPHRINE HYDROCHLORIDE (EPINEPHRINE) EPINEPHRINE0.1 mg  in 1 mL
LIDOCAINE HYDROCHLORIDE (LIDOCAINE) LIDOCAINE50 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
CHLOROBUTANOL 
EDETATE SODIUM 
SODIUM METABISULFITE 
Packaging
#Item CodePackage Description
1NDC:67194-005-0159 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34601/20/2016
Labeler - Unit Dose, Ltd. (119080393)

 
Unit Dose, Ltd.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.