Label: LIGHTS INSTANT STING RELIEF PAD- benzocaine solution

  • NDC Code(s): 61333-214-01
  • Packager: Lights Medical Manufacture Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated September 4, 2024

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  • Active Ingredient

    Benzocaine 6% w/v

    SD Alcohol: 60% w/v

  • Purpose

    Topical Anesthetic

    Antiseptic

  • INDICATIONS & USAGE

    Uses: For temporary relief of pain and itching associated with minor burns, sunburns, minor cut, scrapes, insect bites, or minor skin irritations

  • WARNINGS

    Warnings:

    For external use only. Flammable, keep away from fire or flame. Avoid contact with eyes, if this happens, rinse throughly with water. DO NOT USE with electrocautery procedures.

  • STOP USE

    Stop use and ask a doctor if

    • irritation or redness develops
    • if condition worsens or persists for more than 7 days, or clear up and occur again within a few days, consult a physician
  • KEEP OUT OF REACH OF CHILDREN

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

  • Directions

    For adults and children 2 yeas of age or older: Apply to affected area not more than 3-4 times daily

    Children under 2 yeas of age: Consult a doctor before use

  • Other Information

    Store at room temperature 15-30 C (59-86F). Avoid excessive heat.

  • INACTIVE INGREDIENT

    Inactive Ingredient

    Purified Water

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    LIGHTS INSTANT STING RELIEF PAD 
    benzocaine solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61333-214
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE6 g  in 100 g
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL60 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61333-214-01100 in 1 BOX09/03/2024
    10.8 g in 1 PATCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01709/03/2024
    Labeler - Lights Medical Manufacture Co., Ltd. (529128649)
    Registrant - Lights Medical Manufacture Co., Ltd. (529128649)
    Establishment
    NameAddressID/FEIBusiness Operations
    Lights Medical Manufacture Co., Ltd.529128649manufacture(61333-214)
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