Neuropathy Pain Relief Cream

Manufacturer
Owell Naturals Brand, LLC | Amish Origins LLC
Effective date
2026-01-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:33:42

Label at a glance#

ProductNeuropathy Pain Relief Cream
Active ingredientMENTHOL, UNSPECIFIED FORM
Label structure13 sections

Dosage and administration

Apply a thin layer to the affected area up to 3 to 4 times daily. Massage gently into skin until fully absorbed. For external use only.

Label contents#

Full prescribing information#

PURPOSE

OTC - PURPOSE SECTION

Menthol 4% ..................................................... Topical analgesic

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 8% ..................................................... Topical analgesic

using

OTC - WHEN USING SECTION

Temporarily relieves minor aches and pains of muscles and joints associated with arthritis, backache, strains, sprains, and bruises.

Question?

OTC - QUESTIONS SECTION

call 1+8453228190

Warnings

WARNINGS SECTION

For external use only.
Do not use on wounds or damaged skin.
Avoid contact with eyes or mucous membranes.
Do not bandage tightly or use with a heating pad.
Stop use and ask a doctor if condition worsens or symptoms persist for more than 7 days.
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.

Direction

INSTRUCTIONS FOR USE SECTION

Adults and children 12 years and older:
Apply to affected area not more than 3 to 4 times daily.
Children under 12 years:
Ask a doctor.

Inactive ingredent

INACTIVE INGREDIENT SECTION

Inactive ingredients: Water, Carbomer, Glycerin, Aloe Vera Leaf Juice, Polysorbate 20, Triethanolamine, Arnica, MSM, Vitamin B6, Vitamin E

Indications

INDICATIONS & USAGE SECTION

Temporarily relieves minor aches and pains of muscles and joints associated with arthritis, backache, strains, sprains, and bruises.

keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.

Dosage and Administration

DOSAGE & ADMINISTRATION SECTION

Apply a thin layer to the affected area up to 3 to 4 times daily.
Massage gently into skin until fully absorbed.
For external use only.

Indications & Usage

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains of muscles and joints associated with arthritis, backache, strains, sprains, and neuropathic pain.

principle display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

principal Display panelprincipal Display panelOweli Naturals®
Neuropathy Pain Relief Cream
Menthol 8%
Topical Analgesic

Net Wt 2 fl oz (59 mL)

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Neuropathy Pain Relief Cream
Menthol 4%
Topical Analgesic
Net Wt 2 fl oz (59 mL)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83570-002-01Neuropathy Pain Relief Cream100 g in 1 TUBECREAM1001

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83570-00283570-002-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
MENTHOL, UNSPECIFIED FORML7T10EIP3AACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Neuropathy Pain Relief CreamMENTHOL CREAMOwell Naturals Brand, LLC48979093-2992-5fd8-e063-6394a90a815d2026-01-17WarningsExact identifier
ndc (package): 83570-002-01
ndc (product): 83570-002
ndc11 (package): 83570000201
spl id: 48979093-2993-5fd8-e063-6394a90a815d
spl set id: 48979093-2992-5fd8-e063-6394a90a815d

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.