NUMQUICK TOPICAL ANALGESIC- epinephrine hydrochloride, lidocaine hydrochloride gel 
Unit Dose, Ltd.

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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

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

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:

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:

Outer

NUMQUICK TOPICAL ANALGESIC 
epinephrine hydrochloride, lidocaine hydrochloride gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67194-005
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
EPINEPHRINE HYDROCHLORIDE (UNII: WBB047OO38) (EPINEPHRINE - UNII:YKH834O4BH) EPINEPHRINE0.1 mg  in 1 mL
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE50 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CHLOROBUTANOL (UNII: HM4YQM8WRC)  
EDETATE SODIUM (UNII: MP1J8420LU)  
SODIUM METABISULFITE (UNII: 4VON5FNS3C)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:67194-005-0159 mL in 1 BOTTLE; Type 0: Not a Combination Product01/20/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01501/20/2016
Labeler - Unit Dose, Ltd. (119080393)

Revised: 10/2023
Document Id: 0814b5f6-6da8-6220-e063-6394a90ae05e
Set id: 3f64cbd3-6745-4397-9767-3adc3b301e0e
Version: 4
Effective Time: 20231019
 
Unit Dose, Ltd.