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Antiseptic by Unifirst First Aid Corporation

Medically reviewed on May 18, 2018

Dosage form: liquid
Ingredients: ALCOHOL 500mg in 1g, LIDOCAINE HYDROCHLORIDE 20mg in 1g
Labeler: Unifirst First Aid Corporation
NDC Code: 47682-231

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.

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 – 10 count box

MEDI-FIRST®

Sting Relief Wipes

Product # 23112

NET CONTENTS: 10 units per box

ANTISEPTIC 
alcohol, lidocaine hydrochloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-231
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL500 mg  in 1 g
LIDOCAINE HYDROCHLORIDE (LIDOCAINE) LIDOCAINE HYDROCHLORIDE ANHYDROUS20 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE 
MENTHOL 
WATER 
Packaging
#Item CodePackage Description
1NDC:47682-231-1210 PACKET in 1 BOX
1NDC:47682-231-990.8 g in 1 PACKET
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/FEIOperations
Safetec of America, Inc.874965262manufacture(47682-231)

 
Unifirst First Aid Corporation

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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