Drug Facts

Active ingredient

Epinephrine HCl 0.1 mg

Lidocaine HCl 50 mg

Purpose

Vasoconstrictor

Anesthetic

Uses:

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

Warnings

External use only

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

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 chloride, Sodium metabisulfite

Questions?

Call Toll Free 888/664-9990

Package Labeling:

NUMQUICK ANALGESIC
epinephrine hydrochloride, lidocaine hydrochloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:67194-008
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
EPINEPHRINE HYDROCHLORIDE (UNII: WBB047OO38) (EPINEPHRINE - UNII:YKH834O4BH)	EPINEPHRINE HYDROCHLORIDE	0.1 mg in 1 mL
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	50 mg in 1 mL

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

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:67194-008-01	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/20/2016

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M015	01/20/2016

Labeler - Unit Dose, Ltd. (119080393)

Numquick Analgesic