Label: KROGER PAIN RELIEF LIDOCAINE PATCH- lidocaine patch

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 17, 2024

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

  • Active Ingredient

    Lidocaine 4%

  • Purpose

    Topical anesthetic

  • Use

    Temporary relieves minor pain

  • Warnings

    For external use only

  • Do not Use

    1. more than 1 patch on your body at a time

    2. on cut, irritated or swollen skin

    3. On puncture wounds

    4. For more than one week without consulting a doctor

    5. If you are allergic to any active or inactive ingredients

    if pouch is damaged or opened

  • When using this product

    1. Use only as directed

    2. Read and follow all directions and warnings on this carton

    3. Do not allow contact with the eyes

    4. Do not use at the same time as other topical analgesics

    5. Do not bandage tightly or apply local heat (such as heating pads) to the area of use

    6. Do not microwave

    7. Dispose of used patch in manner that always keeps product away from children or pets. Used patches still contain the drug product that can produce serious adverse effects if a child or pet chews or ingests this patch.

  • Stop use and consult a doctor

    1. condition worsens

    2. redness is present

    3. irritation develops

    4. symptoms persist for more than 7 days or clear up and occur again within a few days

    5. you experience signs of skin injury, such as pain, swelling, or blistering where the product was applied

  • If pregnant or breastfeeding

    ask a health professional before use

  • Keep out of reach of children and pets

    If swallowed, get medical help or contact a Poison Control Center 1-800-222-1222 right away

  • Directions

    1. clean and dry affected area

    2. carefully remove backing from patch starting at the corner

    3. Apply sticky side of patch to affected area.

    4. Use one patch for up to 12 hours.

    5. Discard patch after single use

    children under 12 years or age: consult a physician

  • Other Information

    Store in a clean, dry place outside of direct sunlight. Protect from excessive moisture

  • Inactive Ingredients

    aluminum glycinate, carboxymethylcellulose sodium, glycerin, iodopropynyl butylcarbamate, kaolin, petrolatum, phenoxyethanol, polyacrylic acid, polysorbate 80, povidone, propylene glycol, sodium polyacrylate, tartaric acid, titanium dioxide, water, 3-(2-ethylhexyloxy)propane-1,2-diol

  • Kroger Pain Relief 4% Lidocaine Patch

    label

  • INGREDIENTS AND APPEARANCE
    KROGER PAIN RELIEF LIDOCAINE PATCH 
    lidocaine patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:30142-583
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE4 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    KAOLIN (UNII: 24H4NWX5CO)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    POLYACRYLIC ACID (8000 MW) (UNII: 73861X4K5F)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)  
    TARTARIC ACID (UNII: W4888I119H)  
    POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:30142-583-066 in 1 CARTON04/01/2023
    11 g in 1 PATCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01704/01/2023
    Labeler - Kroger Company (006999528)
    Establishment
    NameAddressID/FEIBusiness Operations
    Foshan Aqua Gel Biotech LLC529128763manufacture(30142-583)