PAIN RELIEF PATCH- camphor, methyl salicylate, menthol patch

Pain Relief Patch by

Drug Labeling and Warnings

Pain Relief Patch by is a Otc medication manufactured, distributed, or labeled by CDMA, Inc., Foshan Aqua Gel Biotech Co., Ltd.,. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Camphor 3.1% - Topical analgesic

Menthol 6.0% - Topical analgesic

Methyl Salicylate 10.0% - Topical analgesic

Purpose

Topical analgesic

Uses

Temporary relief of minor aches and pains of muscles and joints: arthritis, simple backache, muscle strains, muscle sprains, and bruises.

Warnings

For external use only.

Allergy alert: If prone to allergic reaction from aspirin or salicylates, consult a doctor before use.

Directions

Adults and children 12 years of age and over: Clean and dry affected area, free of lotions, ointments and creams. Remove patch from film, apply to affected area. Do not use more than one patch in an 8 hour period. Repeat as necessary. Maximum 3 patches per day. Discard patch after single use. Reseal pouch after opening.

Children under 12 years of age: Consult a physician.

Other Information

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

Inactive Ingredients

Hydrogenated poly

Pentaerythrityl tetra-di-t-butyl hydroxyhydrocinnamate

Petroleum

Styrene/isoprene copolymer

KEEP OUT OF REACH OF CHILDREN

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

PREGNANCY OR BREAST FEEDING

If pregnant or breastfeeding, ask a health professional before use.

STOP USE

Stop use and consult a doctor if rash, itching or excessive skin irritation develops, condition worsens, symptoms last more than 7 days or clear up and occur again within a few days.

DO NOT USE

Do not use more than one patch on your body at a time, on wounds or damaged skin, with a heating pad, or if you are allergic to any ingredients of this product.

WHEN USING

When using this product: Use only as directed, avoid contact with eyes, mucous membranes or rashes, do not bandage tightly, do not use at the same time as other topical analgesics.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PAIN RELIEF PATCH 
camphor, methyl salicylate, menthol patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83324-255
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	3.1 g
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	6 g
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	10 g

Inactive Ingredients
Ingredient Name	Strength
HYDROGENATED C6-20 POLYOLEFIN (100 CST) (UNII: 39EYQ1W9RB)
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
LIQUID PETROLEUM (UNII: 6ZAE7X688J)
STYRENE/ISOPRENE COPOLYMER (28:72; 210000 MW) (UNII: H58HX2GWJ5)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83324-255-60	60 in 1 PACKAGE; Type 0: Not a Combination Product	07/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	07/01/2025

Labeler - CDMA, Inc. (011920774)

Establishment
Name	Address	ID/FEI	Business Operations
Foshan Aqua Gel Biotech Co., Ltd.,		529128763	manufacture(83324-255)