NEKVNRO PAIN RELIEF CREAM- pain relief cream cream

Nekvnro Pain Relief Cream by

Drug Labeling and Warnings

Nekvnro Pain Relief Cream by is a Otc medication manufactured, distributed, or labeled by Guoyu Trading Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Arnica montana HPUS 7%

Purpose

Relieves muscle pain &stiffness, swelling from injuries, discoloration from bruises

Use

temporarily relieves muscle pain and stiffness due to：
■minor injuries

■overexertion

■falls reduces symptoms of bruising such as:

■pain ■swelling

■discoloration

Warnings

For external use only,Do not use if you are allergic to dermfree.cream or to any of this product's inactive ingredients

Do not use

if you are allergic to dermfree.cream or to any of this product's inactive ingredients

When Using

this product avoid contact with eyes, mucous membranes, wounds, damaged or irritated skin. use only as directed dryness or irritation may occur
do not tightly wrap or bandage the treated area
do not apply heat or ice to treated area immediately before or after use

Stop Use

ocondition persists for more than 3 days or worsens
osymptoms clear up and occur again within a few days.

Ask Doctor

ocondition persists for more than 3 days or worsens
osymptoms clear up and occur again within a few days.

Keep Oot Of Reach Of Children

if swallowed，get medical help Or contact a poison Control Center right away.

Directions

Apply a thin layer of dermfree cream to the affected area as soon as possible after minor injury. Repeat 3 times a day or as needed. If heat or ice is applied， wait 5 minutes before applying dermfree cream.

Inactive ingredients

purified water,Alcohol, carbomer,sodium hydroxide, Vanillyl butyl ether

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NEKVNRO PAIN RELIEF CREAM 
pain relief cream cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84844-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW)	ARNICA MONTANA	7 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
WATER (UNII: 059QF0KO0R)
CARBOMER (UNII: 0A5MM307FC)
VANILLYL BUTYL ETHER (UNII: S2ULN37C9R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84844-003-01	80 g in 1 BOTTLE; Type 0: Not a Combination Product	10/23/2024
2	NDC: 84844-003-02	100 g in 1 BOTTLE; Type 0: Not a Combination Product	10/23/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	10/23/2024

Labeler - Guoyu Trading Co., Ltd. (963348600)

Establishment
Name	Address	ID/FEI	Business Operations
Guoyu Trading Co., Ltd.		963348600	manufacture(84844-003)