FDA.reportPublic FDA data

Menthol Pain Relieving Gel

Manufacturer
NeilMed Pharmaceuticals Inc
Effective date
2026-05-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:56:31

Label at a glance#

ProductMenthol Pain Relieving Gel
Active ingredientMENTHOL
Label structure15 sections

Indications and uses

Temporary relief of minor pains of muscle and joints associated with simple backache arthritis sprains, strains or bruises

Dosage and administration

Adults and Childern 2 years and older Clean skin thoroughly. Apply liberally to affected area not more than3-4 times daily. No Protective cover needed. May be used with ice packs. May be used with wet or dry bandages, but wrap loosely. Childern under 2 years of age.

Label contents#

Full prescribing information#

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Drug FactsDrug FactsActive Ingredient- Methanol 2 %

Purpose- External Pain Reliever

Uses

OTC - PURPOSE SECTION

Temporary relief of minor pains of muscle and joints associated with

  • simple backache
  • arthritis
  • sprains, strains or bruises

UsesUses

Warnings

WARNINGS SECTION

For External Use Only.

Avoid Contact with eyes.

WarningsWarnings

Do not Use

OTC - DO NOT USE SECTION

Internally
with heating pads or devices
on wound or damaged skin

Do not UseDo not Use

Ask a doctor before use

OTC - ASK DOCTOR SECTION

if have sensitive skin

Ask a doctorAsk a doctor

Stop Use and Ask a Doctor if

OTC - STOP USE SECTION

condition worses

symptoms last more than 7 days, oe clear up and occur again within a few days

redness or irritaion develops

Stop Use and Ask a doctorStop Use and Ask a doctor

When Using this Product

OTC - WHEN USING SECTION

Use Only as Directed

do not bandage tightly

Avoid contact within eyes and mucos membranes

When Using this ProductWhen Using this Product

If Prgenant or Breast Feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

Ask a healthcare professional before use

Pregnant or Breast feedingPregnant or Breast feeding

Keep Out of the Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Incase of accidental ingestion, get medical help or contact a poison control center immediately

Keep Out of the childernKeep Out of the childern

Directions

INSTRUCTIONS FOR USE SECTION

Adults and Childern 2 years and older

Clean skin thoroughly.

Apply liberally to affected area not more than3-4 times daily.

No Protective cover needed.

May be used with ice packs.

May be used with wet or dry bandages, but wrap loosely.

Childern under 2 years of age.

DirectionsDirections

Other Information

OTHER SAFETY INFORMATION

Store 59°-86°F (15°-30°C)

Keep tightly closed

Do not use, pour, spill or store near heat or open flame.

Other InformationOther Information

Store 59°-86°F (15°-30°C)

Keep tightly closed

Do not use, pour, spill or store near heat or open flame.

Other Ingredients

INACTIVE INGREDIENT SECTION

Camphor

Carbomer

FD&C Blue #1

Isopropyl Alcohol

Propylene Glycol

Purified Water

Sodium Hydroxide

Other IngredientsOther Ingredients

Indications

INDICATIONS & USAGE SECTION

Cooling, Pain relieving gel for muscle aches

arthiritis pain

simple backache

IndicationsIndications

Dosage and Administration

DOSAGE & ADMINISTRATION SECTION

Menthol 2 %

Therapeutic

Greaseless

Net Wt- 8 FL OZ (227 g)

Dosage and AdministrationDosage and Administration

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NeilMed Menthol Pain Relieving Gel

Therapeutic

Greeseless

Cooling, pain, relieving gel for muscle aches,

arthiritis pain,

Simple backache

Package labelPackage label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
311502menthol 2 % Topical GelPSN1
311502menthol 0.02 MG/MG Topical GelSCD1
311502menthol 2 % Topical GelSY1
311502menthol 2 % topical stickSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
13709-357-01Menthol Pain Relieving Gel1 in 1 CARTONGEL11
13709-357-01Menthol Pain Relieving Gel227 g in 1 TUBEGEL2271

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
13709-35713709-357-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
MENTHOLL7T10EIP3AACTIB
CAMPHOR (NATURAL)N20HL7Q941IACT
CARBOMER0A5MM307FCIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
ISOPROPYL ALCOHOLND2M416302IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
WATER059QF0KO0RIACT
SODIUM HYDROXIDE55X04QC32IIACT

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
Menthol Pain Relieving GelPAIN RELIEVING GELNeilMed Pharmaceuticals Inc513a206c-bbf6-3e51-e063-6294a90adf7a2026-05-07WarningsExact identifier
ndc (package): 13709-357-01
ndc (product): 13709-357
ndc11 (package): 13709035701
spl id: 513a206c-bbf7-3e51-e063-6294a90adf7a
spl set id: 513a206c-bbf6-3e51-e063-6294a90adf7a

Reported adverse events (FAERS/openFDA)#

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