NEKVNRO PFERDEBALSAM (arnica montana(arnica) 7%, hamamelis virginiana- witch hazel 2.5% pferdebalsam gel

Nekvnro PFERDEBALSAM by

Drug Labeling and Warnings

Nekvnro PFERDEBALSAM 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 (Arnica)7%W/W

Hamamelis Virginiana (Witch Hazel) 2.5%W/W

Purpose

Pain, inflammation
Pain, Fatigue

Use

Natural temporary relief for aches, pains and inflammation from minor injuries, overexertion and fatigue.

Warnings

For external use only.

Do not use on broken skin or open wounds.

Stop and ask a doctor if

Pain Persists for more than 5 days

.lf pain, redness, or swelling worsens

.if new symptoms occur

Do not use

Do not use on damaged or broken skin

When Using

When using this product avoid contact with eyes or mucous membranes

Stop Use

.lf pain, redness, or swelling worsens

.if new symptoms occu

Ask Doctor

Pain Persists for more than 5 days

.lf pain, redness, or swelling worsens

.if new symptoms occur

Keep Oot Of Reach Of Children

lf swallowed, get medicalhelp or contact a poison control center right away.

Directions

Adults and children over the age of 2 years old: Apply generously with gentle rubbing to the affected area 2-3times daily or as needed. Children less than 2 years of age: Consult a doctor.

Other information

If pregnant or Breast-feeding, ask a health professional before use.

Inactive ingredients

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NEKVNRO PFERDEBALSAM 
arnica montana(arnica) 7%, hamamelis virginiana (witch hazel) 2.5% pferdebalsam gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84010-031
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 mL
HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK - UNII:T7S323PKJS)	HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK	2.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
VANILLYL BUTYL ETHER (UNII: S2ULN37C9R)
CARBOMER 1342 (UNII: 809Y72KV36)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84010-031-01	220 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/23/2024
2	NDC: 84010-031-02	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/23/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	09/23/2024

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

Establishment
Name	Address	ID/FEI	Business Operations
Jiangxi Hemei Pharmaceutical Co., Ltd		724892056	manufacture(84010-031)