Label: STING RELIEF- alcohol, lidocaine hydrochloride cloth

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated February 22, 2016

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

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient:

    Ethyl Alcohol 50.0%

    Lidocaine HCl 2.0%

  • Purpose:

    Antiseptic

    Analgesic (pain reliever)

  • Uses

    First aid analgesic to help prevent infection in and provide temporary relief of the pain of:

    • Insect bites and stings
    • Minor scrapes and burns
  • Warnings:

    For external use only. If swallowed, contact a doctor or poison control center immediately.

    Keep out of the reach of children. Flammable, keep away from open flame.

    DO NOT USE:

    • In the eyes
    • If you are allergic to any of the ingredients
    • On raw surfaces, blistered areas, or over large areas of the body

    WHEN USING THIS PRODUCT:

    • Avoid contact with eyes or mucous membranes

    STOP USE AND ASK A DOCTOR IF:

    • Conditions worsen clear up and then recur
    • The condition persists for more than 7 days
    • A rash, allergic reaction, swelling, irritation or infection occur
  • Directions:

    Packets are not child resistant. Tamper evident packaging, do not use if packet is opened or torn.

    Adults and children:
    over 2 years of age:

    Remove stinger carefully, if possible. Remove wipe from packet, clean affected area thoroughly no more than 3 times daily with saturated applicator.

    Children under 2:

    Consult your doctor.

  • Other information:

    Store at room temperature.

  • Inactive ingredients:

    Benzalkonium Chloride, Menthol, Purified Water

  • Questions about this product:

    Call 800-835-2263 with any questions about this product.

  • Principal Display Panel - Carton Label

    19-002

    MISC

    FIRST AID ONLY®

    Sting Relief Wipes

    10 Packets

    Toallitas para aliviar las molestias de picaduras

    10 sobres

    Principal Display Panel - Carton Label
  • Principal Display Panel - Carton Label

    G326

    MISC

    FIRST AID ONLY®

    Sting Relief Wipes

    50 Packets

    Toallitas para aliviar las molestias de picaduras

    50 sobres

    Principal Display Panel - Carton Label
  • Principal Display Panel - Packet Label

    Sting Relief

    Insect Bite Antiseptic
    and Pain Reliever

    1 Premoistened Towlette

    Package Not Child-Resistant

    FIRST AID ONLY®

    www.FirstAidOnly.com

    Fairfield, CT 06824

    1.800.835.2263

    © Acme United Corporation.

    810001-revA

    Principal Display Panel - Packet Label
  • INGREDIENTS AND APPEARANCE
    STING RELIEF 
    alcohol, lidocaine hydrochloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0924-5200
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    alcohol (UNII: 3K9958V90M) (alcohol - UNII:3K9958V90M) alcohol0.50 mL  in 1 mL
    lidocaine hydrochloride (UNII: V13007Z41A) (lidocaine - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS20 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    benzalkonium chloride (UNII: F5UM2KM3W7)  
    menthol (UNII: L7T10EIP3A)  
    water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0924-5200-0210 in 1 BOX03/06/2012
    1NDC:0924-5200-010.9 mL in 1 PACKET; Type 0: Not a Combination Product
    2NDC:0924-5200-0350 in 1 BOX03/06/2012
    2NDC:0924-5200-010.9 mL in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E03/06/2012
    Labeler - Acme United Corporation (001180207)
    Registrant - Safetec of America, Inc. (874965262)
    Establishment
    NameAddressID/FEIBusiness Operations
    Safetec of America, Inc.874965262MANUFACTURE(0924-5200)