Label: HUSH ANESTHETIC- lidocaine spray

  • NDC Code(s): 49947-001-02, 49947-001-04
  • Packager: HUSH Anesthetic
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 13, 2024

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  • Active Ingredients

    Lidocaine HCL 4% w/w

  • Purpose

    Pain Relieving Liquid

  • Uses

    For temporary relief of pain and itching associated with minor cuts or minor skin irritations.

  • Warnings

    For external use only • Avoid contact with eyes

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

  • STOP USE

    Stop use and ask a doctor if condition worsens or if symptoms persist for more than 7 days or clear up and occur again with a few days.

  • DO NOT USE

    Do not use in large quantities, particularly over raw surfaces or blistered areas.

  • Directions

    Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily.  Children under 2 years of age; consult a physician.

  • Other Information

    Protect this product from excessive heat and direct sun.

  • Inactive ingredients

    Acrylates/c10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf Extract, Aqua (Deionized Water), Calendula Officinale Extract, Capyrlyl Glycol, Chamomile (Chamomile Recutita) Extract, Comfrey (Symphytum Officinale) Extract, Disodium EDTA, Glycerin, Green Tea (Camellia Sinensis) Extract, Menthol, Methylisothiazolinone, Propylene Glycol, SD Alcohol 40B, Triethanolamine

  • Questions or Comments?

    Call 305-231-7229 or visit www.hushanesthetic.com

  • PRINCIPAL DISPLAY PANEL

    4oz bottle4oz bottle4oz bottle4oz bottle

  • PRINCIPAL DISPLAY PANEL

    2oz bottle

  • INGREDIENTS AND APPEARANCE
    HUSH ANESTHETIC 
    lidocaine spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49947-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE40 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    MENTHOL (UNII: L7T10EIP3A)  
    CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)  
    CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    COMFREY ROOT (UNII: M9VVZ08EKQ)  
    CARBOMER INTERPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 132584PQMO)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49947-001-04113.4 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product12/01/2012
    2NDC:49947-001-0256.7 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product12/01/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01712/01/2012
    Labeler - HUSH Anesthetic (012011309)
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