NUMQUICK TOPICAL ANALGESIC- epinephrine hydrochloride, lidocaine hydrochloride gel

Numquick Topical Analgesic by

Drug Labeling and Warnings

Numquick Topical 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 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:

INGREDIENTS AND APPEARANCE

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

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
EPINEPHRINE HYDROCHLORIDE (UNII: WBB047OO38) (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)
EDETATE SODIUM (UNII: MP1J8420LU)
SODIUM METABISULFITE (UNII: 4VON5FNS3C)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67194-005-01	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)