Label: ELECTRUM NUMB ANESTHETIC- lidocaine hcl spray

  • NDC Code(s): 76348-600-04
  • Packager: RENU LABORATORIES, INC.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 20, 2024

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    Active Ingredient

    Lidocaine HCl 4%

  • PURPOSE

    Purpose

    Topical Anesthetic

  • INDICATIONS & USAGE

    Uses

    For the temporary relief of pain associated with minor skin procedures

  • WARNINGS

    Warnings

    For external use only

  • DO NOT USE

    Do Not Use

    • on large areas of the body or on cut, irritated or swollen skin
    • on puncture wounds
    • for more than one week without consulting a doctor
  • WHEN USING

    When using this product

    • Use only as directed. Read and follow all directions and warnings on this label.
    • rare cases of serious burns have been reported with products of this type
    • do not bandage or apply local heat (such as heating pads) to the area of use or use with a medicated patch
    • avoid contact with eyes and mucous membranes
    • a transient burning sensation may occur upon applicator but generally disappears in several days

  • STOP USE

    Stop use and ask a doctor if

    • Condition worsens
    • redness is present
    • irritation develops
    • symptoms persist for more than 7 days or clear up and occur again within a few days
    • you experience signs of skin injury, such as pain, swelling, or blistering where the product was applied
  • PREGNANCY OR BREAST FEEDING

    If pregnant or breast-feeding, ask a health professional before use.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children and pets

    • If swallowed, get medical help or contact a poison control center right away
  • DOSAGE & ADMINISTRATION

    Directions

    adults and children over 12 years:

    • apply a thin layer to affected area every 6 to 8 hours, not to exceed 3 applications in a 24 hour period
    • after applying, wash hands with soap and water
    • children 12 years or younger - ask a doctor
  • INACTIVE INGREDIENT

    Inactive Ingredients: Aloe Barbadensis Leaf Powder, Benzyl Alcohol, Deionized Water, Disodium EDTA, Ethyl Alcohol SD 40B, Glycerin

  • STORAGE AND HANDLING

    Other Information:

    Store at 20-25° C (68 - 77°F)

  • QUESTIONS

    Questions?

    574-975-3632

  • PRINCIPAL DISPLAY PANEL

    ELECTRUM SPRAY LABEL

  • INGREDIENTS AND APPEARANCE
    ELECTRUM NUMB ANESTHETIC 
    lidocaine hcl spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76348-600
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS4.48 g  in 112 g
    Inactive Ingredients
    Ingredient NameStrength
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    ALCOHOL (UNII: 3K9958V90M)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76348-600-04112 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product11/23/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01711/23/2020
    Labeler - RENU LABORATORIES, INC. (945739449)
    Establishment
    NameAddressID/FEIBusiness Operations
    RENU LABORATORIES, INC.945739449manufacture(76348-600)