ANTISEPTIC- alcohol, lidocaine hydrochloride liquid 
Unifirst First Aid Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active Ingredients

Ethyl alcohol 50.0%

Lidocaine HCl 2.0%

Purpose

First Aid Antiseptic

Topical Analgesic

Uses

First aid to help prevent infection in minor scrapes and temporary relief of itching of insect bites

Warnings

For external use only. Flammable, keep away from fire or flame.

Do not use

  • over large areas of the body
  • in the eyes
  • over raw or blistered areas

Stop use and ask doctor if conditions worsen or persist for more than 7 days or clear up and occur again within a few days.

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 and older: Apply to cleaned affected area not more than 3 times daily.
  • children under 2 years of age: Consult a doctor.

Inactive ingredients

benzalkonium chloride, menthol, purified water

PRINCIPAL DISPLAY PANEL – packet label

MEDI-FIRST®

Sting Relief

Insect Bite
Antiseptic and Pain Reliever
Contents: 1 single-use, premoistened towelette

Mfd for Medique Products, Fort Myers, FL 33967
800-634-7680 www.mediqueproducts.com

EXP. LOT

PRINCIPAL DISPLAY PANEL – packet label

PRINCIPAL DISPLAY PANEL – 10 count box

MEDI-FIRST®

Sting Relief Wipes

Product # 23112

NET CONTENTS: 10 units per box

PRINCIPAL DISPLAY PANEL – 10 count box
ANTISEPTIC 
alcohol, lidocaine hydrochloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-231
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL500 mg  in 1 g
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS20 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
MENTHOL (UNII: L7T10EIP3A)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-231-1210 in 1 BOX03/06/201209/03/2018
1NDC:47682-231-990.8 g in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E03/06/201209/03/2018
Labeler - Unifirst First Aid Corporation (832947092)
Registrant - Safetec of America, Inc. (874965262)
Establishment
NameAddressID/FEIBusiness Operations
Safetec of America, Inc.874965262manufacture(47682-231)

Revised: 5/2016
Document Id: 331ef380-f4f4-16b3-e054-00144ff88e88
Set id: 5d500b2d-10f5-4c27-9bec-efd533370dfc
Version: 2
Effective Time: 20160518
 
Unifirst First Aid Corporation