RELIEF PATCH- pain relief patch ointment

relief patch by

Drug Labeling and Warnings

relief patch by is a Otc medication manufactured, distributed, or labeled by Guangzhou Baishili Trading Co., Ltd, Quanzhou Kuangmei Trading Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

BORNEOL 25%

CAMPHOR 20%

Health care function

Relieve neck, shoulder, waist, leg pain and promote health.

Usage

Opened the package back lining paper torn off,clean your skin where the discomfort,aim at the knee or discomfort parts were applied,the corresponding around six to eight hours per post.

Matters needing attention

1. The skin lesions were banned, allergic to wormwood careful.

2. During the period of a few people use local have tickling feeling or a red rash,does not affect theuse disappeared gradually after stopping.
3. The use of skin burns is a normal phenomenon.

Unsuitable people

Pregnant women, those allergic to wormwood are prohibited.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Apply one piece at a time, and each piece should be applied for 8 hours

INACTIVE INGREDIENT SECTION

menthol 55%

Dosage & administration section

BORNEOL 25%
CAMPHOR 20%

MENTHOL 55%

Usage: Opened the package back lining paper torn off,clean your skin where the discomfort,aimat the knee or discomfort parts were applied,the corresponding around six to eight hours per post.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

RELIEF PATCH 
pain relief patch ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84727-021
Route of Administration	AURICULAR (OTIC), CONJUNCTIVAL, CUTANEOUS, DENTAL, ELECTRO-OSMOSIS, BUCCAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BORNEOL (UNII: M89NIB437X) (BORNEOL - UNII:M89NIB437X)	BORNEOL	100 mg  in 100 mg

Product Characteristics
Color	yellow	Score	no score
Shape	FREEFORM	Size	100mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84727-021-01	36 in 1 BOX	09/24/2024
1	NDC: 84727-021-05	1 mg in 1 BOX; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	09/24/2024

Labeler - Guangzhou Baishili Trading Co., Ltd (709042161)

Registrant - Quanzhou Kuangmei Trading Co.,Ltd. (841696421)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Baishili Trading Co., Ltd		709042161	manufacture(84727-021)