MQUPIN KNEE PATCH PAIN RELIFE- knee patch pain relife patch

Mqupin Knee Patch Pain Relife by

Drug Labeling and Warnings

Mqupin Knee Patch Pain Relife by is a Otc medication manufactured, distributed, or labeled by Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Camphor 1.5%
Menthol 1%

Purpose

Topical Analgesic

Use

temporarily relieves minor pain associated with:

■arthritis

■muscle strains

■sprains

■bruises

■ joint pain

Warnings

For external use only.

Do not use

do not use at the same time as other topical analgesics

When Using

■ use only as directed

■ do not bandage tighty or use with a heating pad

■ avoid contact with eyes and mucous membranes

■ do not apply to wounds or damaged, broken or imitated skin

■ do not use at the same time as other topical analgesics

Stop Use

■ rash, itching or excessive skin irritation develops

■ condition worsens

■ symptoms persist for more than 7 days

■ symptoms clear up and occur again within a few days If pregnant or breastfeeding, ask a health professional before use

■ Keep out of reach of children

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

Ask Doctor

■ Keep out of reach of children

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

Keep Out Of Reach Of Children

Keep out of reach of children

Directions

adults and children over 12 years:

■clean and dry the affected area

■remove backing from patch and apply patch to affected area

■use 1 patch per knee for 8 to 12 hours, once per day

Other information

store at room temperature, not to exceed 86°F (30°C)

Inactive ingredients

Chili oil, Turpentine, Azone, Cinnamon oil, Jiejin Grass, Anredera Cordifolia，cactus.

Questions

mqupin86@gmail.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MQUPIN KNEE PATCH PAIN RELIFE 
knee patch pain relife patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83781-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BORNEOL (UNII: M89NIB437X) (BORNEOL - UNII:M89NIB437X)	BORNEOL	1.5 g  in 100
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	1 g  in 100

Inactive Ingredients
Ingredient Name	Strength
CINNAMON OIL (UNII: E5GY4I6YCZ)
ANREDERA CORDIFOLIA LEAF (UNII: MGE8MNJ5L6)
TURPENTINE (UNII: XJ6RUH0O4G)
CAPSICUM (UNII: 00UK7646FG)
LAUROCAPRAM (UNII: 1F3X9DRV9X)
HOODIA GORDONII SAP (UNII: K7QNF2DJR8)
GRASS CARP (UNII: 9A3N315I11)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83781-004-01	24 in 1 BOX; Type 0: Not a Combination Product	11/05/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	11/05/2023

Labeler - Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd (701762807)

Establishment
Name	Address	ID/FEI	Business Operations
Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd		701762807	manufacture(83781-004) , label(83781-004)