Neuropathy Cream

Manufacturer
Owell Naturals Brand, LLC | Amish origins LLC
Effective date
2026-01-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:33:30

Label at a glance#

ProductNeuropathy Cream
Active ingredientMENTHOL
Label structure14 sections

Indications and uses

Temporarily relieves minor aches and pains of muscles and joints.

Dosage and administration

adults and children 12 years of age and older: apply to affected area no more than 3 to 4 times daily children under 12 years of age: ask a doctor

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Mentho1 4%

Purpose

OTC - PURPOSE SECTION

Extenal Analgesic

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves minor aches and pains of muscles and joints.

Do not use

OTC - DO NOT USE SECTION

On wound or Damage skin

When using this product

OTC - WHEN USING SECTION

do not get into eyes or mucous membranes
do not bandage tightly

Stop use and ask a doctor if

OTC - STOP USE SECTION

condition worsens
symptoms persist for more than 7 days or clear up and occur again within a few days

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

adults and children 12 years of age and older:
apply to affected area no more than 3 to 4 times daily

children under 12 years of age:
ask a doctor

Questions?

OTC - QUESTIONS SECTION

Questions or comments?
Call 1-800-XXX-XXXX
Manufactured for: Your Company Name
City, State, ZIP

WARNINGS

WARNINGS SECTION

For external use only.

Do not use on:
• Broken skin
• Wounds
• Irritated skin

When using this product:
• Avoid contact with eyes and mucous membranes
• Do not bandage tightly
• Do not apply heat to the treated area

Stop use and ask a doctor if:
• Condition worsens
• Symptoms persist for more than 7 days
• Redness or irritation develops

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

Inactive ingredients: purified water, glycerin

INACTIVE INGREDIENT SECTION

none

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Neuropathy Cream

Menthol 1%

Topical Analgesic

Net Wt. XX oz (XX g)

For external use only

Distributed by:
Owell Naturals Brand, LLC
USA

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

See product Principal Display PanelPrincipal Display Panel label image.

principlal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

see product image principal Display panelprincipal Display panel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1148430menthol 4 % Topical CreamPSN1
1148430menthol 40 MG/ML Topical CreamSCD1
1148430menthol 4 % Topical CreamSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83570-001-01Neuropathy Cream1 g in 1 TUBECREAM11

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83570-00183570-001-01

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
MENTHOLL7T10EIP3AACTIB

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 CreamMENTHOL CREAMOwell Naturals Brand, LLC48739205-627b-41d0-e063-6394a90a34622026-01-15WarningsExact identifier
ndc (package): 83570-001-01
ndc (product): 83570-001
ndc11 (package): 83570000101
spl id: 48739205-627c-41d0-e063-6394a90a3462
spl set id: 48739205-627b-41d0-e063-6394a90a3462

Reported adverse events (FAERS/openFDA)#

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