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Lidocaine Hydrochloride by Unifirst First Aid Corporation

Medically reviewed on June 11, 2018

Dosage form: spray
Ingredients: Lidocaine Hydrochloride 20g in 1L
Labeler: Unifirst First Aid Corporation
NDC Code: 47682-308

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 ingredient

Lidocaine HCl 2.0%

Purpose

Topical pain relief

Uses

Temporary pain relief associated with minor bums

Warnings

For external use only.

Do not use
  • in large quantities, particularly over raw or blistered areas
  • near eyes, if this happens rinse thoroughly with water

Stop use and ask a doctor if condition worsens or persists for more than 7 days or clears up and returns.

Keep out of reach of children. If swallowed get medical help or contact a Poison Control Center right away.

Directions
  • spray an even layer of bum spray over cleaned affected area not more than 3-4 times daily
  • not to be used on children under 12 years of age

Inactive ingredients

aloe vera, germaben II, propylene glycol, purified water

Questions or comments?

1-800-634-7680

Principal Display Panel - Bottle Label

NDC 47682-308-02

Burn
Spray

Analgesic

  • relieves pain of minor burn, sunburn,
    scalds and abrasions
  • provides a disinfecting action

GREEN GUARD

2 Fl. Oz. (59.1 ML)

LIDOCAINE HYDROCHLORIDE 
lidocaine hydrochloride spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-308
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Lidocaine Hydrochloride (Lidocaine) Lidocaine Hydrochloride Anhydrous20 g  in 1 L
Inactive Ingredients
Ingredient NameStrength
aloe vera leaf 
propylene glycol 
diazolidinyl urea 
water 
Packaging
#Item CodePackage Description
1NDC:47682-308-020.0591 L in 1 BOTTLE, PUMP
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34806/10/2015
Labeler - Unifirst First Aid Corporation (832947092)
Registrant - Safetec of America, Inc. (874965262)
Establishment
NameAddressID/FEIOperations
Safetec of America, Inc.874965262MANUFACTURE(47682-308)

 
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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