NUMQUICK ANALGESIC- epinephrine, lidocaine hydrochloride solution

Numquick Analgesic by

Drug Labeling and Warnings

Numquick Analgesic by is a Otc medication manufactured, distributed, or labeled by Unit Dose, Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

(-) Epinephrine 0.01% w/w

:Lidocaine HCL 5% w/w

Purpose

Vasoconstrictor

Local Anesthetic

Uses:

Temporarily relieves local discomfort or pain and swelling 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 mechanical device or applicator

When Using This Product

do not use more than directed.

Stop use and ask a doctor

if pain worsens or does not improve in 7 days

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

Keep out of the reach of children.

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

Directions:

Adults and Children over age 12 ​---​ Spray 1-2ml to clean, dry affected area as needed up to 6 times daily.

Children under age 12: ask a doctor

​Store in a cool, dark place or refrigerate.

Inactive Ingredients:

Aqua (DI Water), Chlorobutanol, Glycerin, Sodium EDTA, Sodium metabisulfite

Questions?

​Call Toll Free 888/452-4946

Package Labeling:

INGREDIENTS AND APPEARANCE

NUMQUICK ANALGESIC 
epinephrine, lidocaine hydrochloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67194-007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
EPINEPHRINE (UNII: YKH834O4BH) (EPINEPHRINE - UNII:YKH834O4BH)	EPINEPHRINE	0.1 mg  in 1 mL
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	50 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CHLOROBUTANOL (UNII: HM4YQM8WRC)
GLYCERIN (UNII: PDC6A3C0OX)
EDETATE SODIUM (UNII: MP1J8420LU)
SODIUM METABISULFITE (UNII: 4VON5FNS3C)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67194-007-01	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/20/2016

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)