BURN N BITE (LIDOCAINE, MENTHOL) GEL [Q.A. LABORATORIES]

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BURN N BITE (LIDOCAINE, MENTHOL) GEL [Q.A. LABORATORIES]
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NDC 52099-9005-1
Set ID 283be206-8d1b-4508-a0a6-67200d78d46c
Category HUMAN OTC DRUG LABEL
Packager Q.A. Laboratories
Generic Name
Product Class Amide Local Anesthetic, Antiarrhythmic
Product Number
Application Number PART348
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  • Drug Facts

  • Active Ingredient

    Lidocaine 2%
    Menthol 1%

  • Purpose

    Ant-itch, Pain Relief

  • Uses

    for the temporary relief of pain and discomfort caused by • minor burns • sunburn • scrapes • insect bites • minor skin irritations • rashes due to poison ivy, oak and sumac.

  • Warnings

    For external use only.

    When using this product

    • Avoid contact with eyes

    Do not use

    • Under bandages or compresses

    Stop use and ask a doctor if condition worsens, or if symptoms 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 of age and older: Apply to the affected area not more than two times daily.

    Children under 2 years of age: Do not use, consult a doctor

  • Inactive Ingredients

    Deionized water, propylene glycol, aloe, isopropyl alcohol, carbomer, triethanolamine, phenoxyethanol

  • Questions or comments:

    858-782-6627, 816-421-8081

    Stanmar Laboratories     

    Division of Q.A. Laboratories

    404 Admiral Boulevard Kansas City, MO 64106

    Ideazbrands.com

    Made in the USA

  • Packaging

    BURN N BITEBURN N BITE

  • INGREDIENTS AND APPEARANCE
    BURN N BITE 
    lidocaine, menthol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52099-9005
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE2 g  in 100 g
    MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ALOE (UNII: V5VD430YW9)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52099-9005-1141 g in 1 TUBE; Type 0: Not a Combination Product03/30/1994
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34803/30/1994
    Labeler - Q.A. Laboratories (065361149)
    Establishment
    NameAddressID/FEIBusiness Operations
    Q.A. Laboratories065361149manufacture(52099-9005)
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