3% MENTHOL PLUS 0.083% CAPSAICIN PAIN RELIEF PATCH- pain relief patch, pain relief strip patch

3% Menthol plus 0.083% Capsaicin Pain Relief Patch by

Drug Labeling and Warnings

3% Menthol plus 0.083% 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]

3% Menthol plus 0.083% Capsaicin Pain Relief Patch, Package NDC Code: 85323-008-01

3% Menthol plus 0.083% Capsaicin Pain Relief Patch, Package NDC Code: 85323-008-01

Active Ingredient

Active Ingredients (in each gram):

Menthol 30mg

Capsaicin 0.83mg

Purpose

Purpose: Topical anesthetic

Uses

Uses

Temporarily relieves minor pain associated with:

• arthritis
• simple backache
• bursitis
• tendonitis
• muscle strains
• bruises
• cramps

Warnings

WARNINGS: EXTERNAL USE ONLY

When using this product

• use only as directed
• do not bandage tightly or use with a heating pad
• aviod contact with eyes and mucous membranes
• do not apply to wounds or damaged skin

Stop use and ask a doctor

• condition worsens
• symptoms persist for more than 7 days or clear up and occur again within a few days
• redness is present
• skin irritation develops

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.

Other information

Other Information

• store at room temperature 68 to 77℉ (20-25℃)

Inactive Ingredients

Glycerin, Sodium Polyacrylate, Dihydroxyaluminum Aminoacetate Anhydrous, Edetate Disodium, Kaolin, Carbomer, Carboxymethylcellulose Sodium, Purified Water, Tartaric Acid, Povidone K90, DMDM Hydantoin, Alcohol 95%, Polysorbate 80, Propylene Glycol.

KEEP OUT OF REACH OF CHILDREN.

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

Directions

DIRECTIONS

Adult and children 12 years of age and older:

• Partially peel back protective film and apply exposed patch to site of pain. Carefully remove remaining film while pressing patch to skin for secure adhesions
• Apply to affected area not more than 3 to 4 times daily

Children under 12 years of age: DO NOT use without consulting a doctor.

Temporarily relieves minor pain associated with:

• arthritis
• simple backache
• bursitis
• tendonitis
• muscle strains
• bruises
• cramps

Adult and children 12 years of age and older:

• Partially peel back protective film and apply exposed patch to site of pain. Carefully remove remaining film while pressing patch to skin for secure adhesions
• Apply to affected area not more than 3 to 4 times daily

Children under 12 years of age: DO NOT use without consulting a doctor.

INGREDIENTS AND APPEARANCE

3% MENTHOL PLUS 0.083% CAPSAICIN PAIN RELIEF PATCH 
pain relief patch, pain relief strip patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85323-008
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	3 g  in 100 g
CAPSAICIN (UNII: S07O44R1ZM) (CAPSAICIN - UNII:S07O44R1ZM)	CAPSAICIN	83 mg  in 100 g

Inactive Ingredients
Ingredient Name	Strength
SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)
ALCOHOL 95% (UNII: 7528N5H79B)
WATER (UNII: 059QF0KO0R)
DIHYDROXYALUMINUM AMINOACETATE ANHYDROUS (UNII: 1K713C615K)
KAOLIN (UNII: 24H4NWX5CO)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
EDETATE DISODIUM (UNII: 7FLD91C86K)
CARBOMER 934 (UNII: Z135WT9208)
TARTARIC ACID (UNII: W4888I119H)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
POVIDONE K90 (UNII: RDH86HJV5Z)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
DMDM HYDANTOIN (UNII: BYR0546TOW)

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85323-008-01	24 in 1 BOX	06/10/2025
1		2 in 1 POUCH
1		8.5 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(85323-008)