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

0.025% Capsaicin Pain relief Patch by

Drug Labeling and Warnings

0.025% Capsaicin Pain relief Patch by is a Otc medication manufactured, distributed, or labeled by Xuzhou Lanting Pharmaceutical Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

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

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 Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85323-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAPSAICIN (UNII: S07O44R1ZM) (CAPSAICIN - UNII:S07O44R1ZM)	CAPSAICIN	0.025 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
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
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85323-005-01	24 in 1 BOX	06/10/2025
1		2 in 1 POUCH
1		6.65 g in 1 PATCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		06/10/2025

Labeler - Xuzhou Lanting Pharmaceutical Co., Ltd (457641059)

Registrant - Xuzhou Lanting Pharmaceutical Co., Ltd (457641059)

Establishment
Name	Address	ID/FEI	Business Operations
Xuzhou Lanting Pharmaceutical Co., Ltd		457641059	manufacture(85323-005)