DERMFREE PAIN RELIEF- arnica montana hpus 7% pain relief cream

DERMFREE PAIN RELIEF by

Drug Labeling and Warnings

DERMFREE PAIN RELIEF by is a Otc medication manufactured, distributed, or labeled by Jiangxi Hemei Pharmaceutical Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Arnica montana HPUS7%

Purpose

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

Use

temporarily relieves muscle pain and stiffness due to:minor injuriesmoverexertionmfalls reduces symptoms of bruisingsuch as:mpainmswellingmdiscoloration

Warnings

For external use only

Do not use

Do not use if you are allergic to dermfreecream or to any of this product's inactive ingredients

When Using

When usingthis product avoid contact with eyes, mucous membranes, woundsdamaged or irritated skin.use only as directed dryness or irritationmay occur
do not tightly wrap or bandage the treated areado not apply heat or ice to treated areaimmediately beforeor after use

Stop Use

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

Ask Doctor

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

Keep Oot Of Reach Of Children

lfswallowed, get medical helpor contact a Poison Control Center right away

Directions

Apply a thin layer of dermfree cream to the affected area assoon as possible after minor injury. Repeat 3 times a day or asneeded.lf heat orice is applied, wait 5 minutes before applyingdermfree cream.

Inactive ingredients

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DERMFREE PAIN RELIEF 
arnica montana hpus 7% pain relief cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84010-016
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
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
ALCOHOL (UNII: 3K9958V90M)
VANILLYL BUTYL ETHER (UNII: S2ULN37C9R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84010-016-01	85 g in 1 JAR; Type 0: Not a Combination Product	05/07/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	05/07/2024

Labeler - Jiangxi Hemei Pharmaceutical Co., Ltd (724892056)

Establishment
Name	Address	ID/FEI	Business Operations
Jiangxi Hemei Pharmaceutical Co., Ltd		724892056	manufacture(84010-016)