Label: LIDOCAINE HYDROCHLORIDE spray

  • NDC Code(s): 47682-308-02
  • Packager: Unifirst First Aid Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 16, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredient

    Lidocaine HCl 2.0%

  • PURPOSE

    Purpose

    External analgesic

  • INDICATIONS & USAGE

    Uses

    Temporary pain relief for minor bums

  • WARNINGS

    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.

  • DOSAGE & ADMINISTRATION

    Directions

    • adults and children 2 years of age and older: spray an even layer of bum spray over cleaned affected area not more than 3-4 times daily
    • for children under 2 years of age consult a physician
  • OTHER SAFETY INFORMATION

    Other information

    • store at room temperature
  • INACTIVE INGREDIENT

    Inactive ingredients

    aloe vera, germaben II, propylene glycol, purified water

  • QUESTIONS

    Questions or comments? 1-800-634-7680

  • Green Guard Burn Spray Label

    Burn
    Spray

    Lidocaine HCl 2.0%

    Topical Pain Relief

    relieves pain of minor burn

    Store at room temperature

    GREEN GUARD

    2 fl oz (59.1 ML)

    3011

  • INGREDIENTS AND APPEARANCE
    LIDOCAINE HYDROCHLORIDE 
    lidocaine hydrochloride spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-308
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS20 g  in 1 L
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47682-308-020.0591 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product06/10/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01506/10/2015
    Labeler - Unifirst First Aid Corporation (832947092)
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