MEDI-FIRST STING RELIEF- benzocaine 6%, isopropyl alcohol 60% swab

Medi-First Sting Relief by

Drug Labeling and Warnings

Medi-First Sting Relief by is a Otc medication manufactured, distributed, or labeled by Unifirst First Aid Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Benzocaine 6% w/v

Isopropyl alcohol 60% w/v

Purpose

Topical anesthetic

Antiseptic

Uses

For temporary relief of pain and itching associated with minor burns, scrapes and insect bites.

Warnings

For external use only.

Flammable, keep away from fire or flame.

Do not use

• in the eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if

• irritation, redness or other symptoms develop
• the condition persists or gets worse

Keep out of reach of children.

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

Directions

Adults and children 2 years of age and older: Apply to affected area 3-4 times daily.

Children under 2 years: CXonsult physician.

Other information

• store at room temperature 59º-86ºF (15º-30ºC)
• tamper evident sealed packets
• do not use any opened or torn packets

Inactive ingredients

purified water

Questions or comments?

1-800-634-7680

Medi-First Sting Relief Wipes Label

Medi-First®

Sting Relief Wipes

Benzocaine/ Isopropyl Acohol

Topical Anesthetic/ Antiseptic

Product # 23112

NET CONTENTS: 10 wipes per box

INGREDIENTS AND APPEARANCE

MEDI-FIRST STING RELIEF 
benzocaine 6%, isopropyl alcohol 60% swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47682-234
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	60 mg  in 1 mL
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	0.6 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47682-234-99	0.6 mL in 1 PACKET; Type 0: Not a Combination Product	07/02/2018
2	NDC: 47682-234-12	10 in 1 BOX	07/02/2018
2		0.6 mL in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	07/02/2018

Labeler - Unifirst First Aid Corporation (832947092)