Label: 0.025% CAPSAICIN PAIN RELIEF PATCH- capsaicin pain relief patch, capsaicin pain relief strip patch

  • NDC Code(s): 85323-005-01
  • Packager: Xuzhou Lanting Pharmaceutical Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 10, 2025

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

  • 0.025% Capsaicin Pain relief Patch, Package NDC Code: 85323-005-01

    0.025% Capsaicin Pain relief Patch, Package NDC Code: 85323-005-01

    0.025 Capsaicin Pain relief Patch 85323-005-01

    0.025 Capsaicin Pain relief Patch 85323-005-pouch

    Active Ingredient

    Active Ingredient: 0.025% Capsaicin

    Purpose

    Purpose: Topical anesthetic

    Warnings

    Warnings: For external use only

    Do not use

    • on wounds or damaged skin
    • with a heating pad
    • with or at the same times as other external analgesic
    • if you are allergic to any ingredients of this product

    When using this product

    • do not use otherwise than as directed
    • avoid contact with the eyes, mucous membranes or rashes
    • do not bandage tightly
    • discontinue use at least 1 hour before a bath or shower
    • do not use immediately after a bath or shower

    Stop use and ask a doctor if

    • rash, itching or excessive skin irritation develops
    • condition worsen
    • symptoms persist for more than 7 days
    • symptoms clear up and occur again within few days

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

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.

    Uses

    For temporary relief of minor aches and pains of muscles & joints associated with:

    • Simple Backache
    • Arthritis
    • Strains
    • Bruises
    • Sprains

    Other information

    Other Information

    • Avoid storing product in direct sunlight
    • Protect product from excessive moisture

    Inactive Ingredients

    Glycerin, Sodium Polyacrylate, Dihydroxyaluminum Aminoacetate Anhydrous, Edetate Disodium, Kaolin, Propylene Glycol, Polysorbate 80, Carboxymethylcellulose Sodium, Carbomer, Purified Water, POVIDONE K90, Tartaric Acid, Dmdm Hydantoin.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.

    For temporary relief of minor aches and pains of muscles & joints associated with:

    • Simple Backache
    • Arthritis
    • Strains
    • Bruises
    • Sprains

    Adult and children 12 years of age and over:

    • Clean and dry affected area
    • Remove patch from film
    • Apply to affected area not more than 3 to 4 times daily
    • Remove patch from skin after at most 8 hours of application

    Children under 12 years of age: consult a doctor.

    Directions

    Adult and children 12 years of age and over:

    • Clean and dry affected area
    • Remove patch from film
    • Apply to affected area not more than 3 to 4 times daily
    • Remove patch from skin after at most 8 hours of application

    Children under 12 years of age: consult a doctor.

  • INGREDIENTS AND APPEARANCE
    0.025% CAPSAICIN PAIN RELIEF PATCH 
    capsaicin pain relief patch, capsaicin pain relief strip patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:85323-005
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAPSAICIN (UNII: S07O44R1ZM) (CAPSAICIN - UNII:S07O44R1ZM) CAPSAICIN0.025 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    KAOLIN (UNII: 24H4NWX5CO)  
    CARBOMER 934 (UNII: Z135WT9208)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    DIHYDROXYALUMINUM AMINOACETATE ANHYDROUS (UNII: 1K713C615K)  
    WATER (UNII: 059QF0KO0R)  
    TARTARIC ACID (UNII: W4888I119H)  
    POVIDONE K90 (UNII: RDH86HJV5Z)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:85323-005-0124 in 1 BOX06/10/2025
    12 in 1 POUCH
    16.65 g in 1 PATCH; Type 0: Not a Combination Product
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)06/10/2025
    Labeler - Xuzhou Lanting Pharmaceutical Co., Ltd (457641059)
    Registrant - Xuzhou Lanting Pharmaceutical Co., Ltd (457641059)
    Establishment
    NameAddressID/FEIBusiness Operations
    Xuzhou Lanting Pharmaceutical Co., Ltd457641059manufacture(85323-005)