Numquick Topical Analgesic

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

Medically reviewed by Drugs.com. Last updated on Dec 12, 2022.

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 Type	HUMAN OTC DRUG	Item Code (Source)	NDC:67194-005
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
EPINEPHRINE HYDROCHLORIDE (EPINEPHRINE)	EPINEPHRINE	0.1 mg in 1 mL
LIDOCAINE HYDROCHLORIDE (LIDOCAINE)	LIDOCAINE	50 mg in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER
CHLOROBUTANOL
EDETATE SODIUM
SODIUM METABISULFITE

Packaging
#	Item Code	Package Description
1	NDC:67194-005-01	59 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part346	01/20/2016

Labeler - Unit Dose, Ltd. (119080393)

Document Id: 60e28167-aab8-3d6e-e053-2a91aa0a342f

Set id: 3f64cbd3-6745-4397-9767-3adc3b301e0e

Version: 3

Effective Time: 20171221

Unit Dose, Ltd.

Further information

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

Medical Disclaimer

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