0.025% CAPSAICIN PAIN RELIEF PATCH- capsaicin pain relief patch, capsaicin pain relief strip patch 
Xuzhou Lanting Pharmaceutical Co., Ltd

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85323-005, 0.025% Capsaicin Pain relief Patch

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.

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)

Revised: 6/2025
Document Id: 3d3c4563-2565-ddcd-e063-6294a90ae4d9
Set id: 37776daf-c8ff-167f-e063-6294a90aedbb
Version: 3
Effective Time: 20250610
 
Xuzhou Lanting Pharmaceutical Co., Ltd