DERMFREE NEUROPATHY- arnica montana 1x hpus 7% neuropathy cream

DERMFREE NEUROPATHY by

Drug Labeling and Warnings

DERMFREE NEUROPATHY 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 1X HPUS 7%

Purpose

Neuropathy, Tingling, Burning and Numbness Symptom Relief Muscle Pain, Neuralgia, Stiffness, Swelling， Bruising Symptom Relief

Use

Symptomatic treatment of neuropathy, tingling， burning and numbness.

Warnings

For external use only.
Ask a doctor before use if pregnant or nursing
Avoid contact with eyes.

Do not use

by mouth, in nostrils, on wounds or damaged skin.

When Using

When using this product avoid contact with eyes

Stop Use

Discontinue use if irritation occurs.

Ask Doctor

Discontinue use ifirritation occurs

Keep Oot Of Reach Of Children

Do not use if tamper evident seal is broken.In case of ingestion call Poison Control Center hotline immediately at 1-800-222-1222.

Directions

Apply to the effected areas 2-3 times daily, massage it and wait foritdry.

Other information

Do not use if tamper evident seal is broken.In case of ingestion call Poison Control Center hotline immediately at 1-800-222-1222.
The letters HPUS indicate the component(s) in this product is (are) officially monographed in the Homeopathic Pharmacopeia of the United States.

Inactive ingredients

Alcohol, carbomer, purifed water,Arnica.sodium hydroxide,Vitamin B6, VitaminE, Vanillyl butyl ether,Msm, Aloe vera

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DERMFREE NEUROPATHY 
arnica montana 1x hpus 7% neuropathy cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84010-033
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
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
WATER (UNII: 059QF0KO0R)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
ALCOHOL (UNII: 3K9958V90M)
PYRIDOXINE (UNII: KV2JZ1BI6Z)
VANILLYL BUTYL ETHER (UNII: S2ULN37C9R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
.ALPHA.-TOCOPHEROL SUCCINATE, D- (UNII: LU4B53JYVE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84010-033-01	100 g in 1 JAR; Type 0: Not a Combination Product	09/25/2024
2	NDC: 84010-033-02	60 g in 1 JAR; Type 0: Not a Combination Product	09/25/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	09/25/2024

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

Establishment
Name	Address	ID/FEI	Business Operations
Jiangxi Hemei Pharmaceutical Co., Ltd		724892056	manufacture(84010-033)