FourPainRX

Manufacturer
Neptune Products LLC
Effective date
2022-11-30
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 21:45:48

Label at a glance#

ProductFourPainRX
Active ingredientCAPSAICIN, METHYL SALICYLATE, MENTHOL, LIDOCAINE HYDROCHLORIDE
Label structure14 sections

Dosage and administration

Adults 18 years and children 12 years and older: apply product directly to affected area product may be used as necessary, but should not be used more than four times per day. wash hands immediately afterwards Children 12 years or younger: ask a doctor

Storage and handling

Store at at 20ºC - 25ºC (68ºF - 77ºF)

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Lidocaine HCL 4%

Methyl Salicylate 27.5%

Menthol 10%

Capsaicin 0.0325%

Active IngredientsActive Ingredients

OTC - PURPOSE SECTION

Topical Anesthetic

Topical NSAID

Topical Analgesic

Counterirritant

PurposePurpose

INDICATIONS & USAGE SECTION

Temporarily relieves minor aches and muscles pains associated with:

  • arthritis
  • simple back pain
  • strains
  • muscle soreness

Instructions for useInstructions for use

WARNINGS SECTION

For external use only

WarningsWarnings

Do not use

OTC - DO NOT USE SECTION

  • on open wounds, cuts, damaged or infected skin
  • with bandage or a heating pad
  • if condition worsens or symptoms persists for more than 7 days
  • excessive skin irritation occurs

Do not useDo not use

Ask a doctor before use if

OTC - ASK DOCTOR SECTION

  • you are allergic to any ingredients, PABA, aspirin products or sulfa
  • Ask Doctor before use itAsk Doctor before use it

OTC - WHEN USING SECTION

  • avoid contact with eyes, genitals, and other mucus membranes. If eye contact occurs, rinse thoroughly with water.

When usingWhen using

If pregnant or breast feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a healthcare professional before use.

PregnancyPregnancy

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away. Package not child resistant.

Keep outKeep out

STORAGE AND HANDLING SECTION

Store at at 20ºC - 25ºC (68ºF - 77ºF)

StoreStore

Directions

DOSAGE & ADMINISTRATION SECTION

Adults 18 years and children 12 years and older:

  • apply product directly to affected area
  • product may be used as necessary, but should not be used more than four times per day.
  • wash hands immediately afterwards

Children 12 years or younger: ask a doctor

directionsdirections

INACTIVE INGREDIENT SECTION

Allantoin, Aloe Barbadensis Leaf Juice, Ammonium Acryloyldimethyltaurate/VP Copolymer, Cetyl Alcohol, Chamomilla Recutita Matricaria Flower Extract, Dimethicone, Disodium EDTA, Ethylhexylglycerin, Glycerin, Glyceryl Stearate, Inulin Lauryl Carbamate, PEG-100 Stearate, Phenoxyethanol, Stearic Acid, Triethanolamine, Water.

Inact ingredientsInact ingredients

For Questions or Comments

OTC - QUESTIONS SECTION

Please Call 800-674-7939

Manufactured in the U.S.A. for:
Neptune Products LLC
Reno, NV 89501

questionsquestions

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 72594-5000-1
FourPainRX™
Physician Formulated Ointment for Pain
Pain Relief Ointment
Lidocaine HCL
Methyl Salicylate
Menthol

Capsaicin
Net WT 4 oz. (121 g)

allall

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72594-5000-1GM - Gram72594-50001231a6fa-27cf-466c-912d-9627474ddc0212022-09-12

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72594-500072594-5000-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

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
0c7b849e-30a2-702e-e063-6394a90a43e9b298fb9c-237b-b3b2-e053-2995a90a0e402023-12-08WarningsExact identifier
spl set id: b298fb9c-237b-b3b2-e053-2995a90a0e40

Reported adverse events (FAERS/openFDA)#

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