Elgin Pain Relief

Manufacturer
Eco-Logics, Inc. | Elginex Corporation | Natural Essentials,Inc.
Effective date
2025-10-18
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 01:39:31

Label at a glance#

ProductElgin Pain Relief
Active ingredientMENTHOL
Label structure14 sections

Indications and uses

Uses: Temporary relief from minor pains of sore muscles and jpintsassociated with arthritis, backache, strains, and sprains..

Dosage and administration

Directions Adults and children 2 years of age and older: Apply to painful muscles and joint. Genthly massage thoroughly into affected area. Repeat as necessary but not more than 4 times daily.

Storage and handling

Other Information: Store in a cool dry place with lid closed tightly.

Label contents#

Full prescribing information#

OTC-ACTIVE INGREDIENT SECTION

OTC - ACTIVE INGREDIENT SECTION

Active Ingedients Purpose

Menthol USP 3.5%................... Topical Analgesic

OTC - PURPOSE SECTION

Menthol USP 3.5% Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

Uses:

Temporary relief from minor pains of sore muscles and jpintsassociated with arthritis, backache, strains, and sprains..

Warning

WARNINGS SECTION

WARNING:

For external use only.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions

Adults and children 2 years of age and older:

Apply to painful muscles and joint. Genthly massage thoroughly into affected area.

Repeat as necessary but not more than 4 times daily.

Ask a doctor before use if you have:

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have Sensitive skin.

When Using this Product:

OTC - WHEN USING SECTION

When Using this product:

Avoid contact with the eyes or muscous membranes

Do not apply to wounds or damaged skin

Do not use with other ointmens, creams, sprays, or linaments.

Do not apply to irritated skin or if excessive irration develops

Do not bandage

Wash hands after use with cool water

Do not use with heating pad or device.

Stop Use and Ask Doctor If:

OTC - STOP USE SECTION

Stop Use and Ask Doctor If: Condition worsens, or if symtoms persist for more than 7 days, or clear up and reoccur.

If pregnant or breast feeding:

OTC - PREGNANCY OR BREAST FEEDING SECTION

If Pregnant or breast feeding: Ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If accidentally ingested, get medicalhelp or contact a Poisan Control Center immediately.

immedaAqueous (Deionized filtered water) blend of certified * Organic Aloe Barbadensis Extract, Isopropyl Alcohol, *IlexParaguariensis leaf extract, Cinnamomum Camphora (camphor),Tocopheryl Avetate (Vitamin E Acetate), Carbomer, FD&C Blue #1, FD&C Yellow #5, Methylparaben, Triethanolamine.

Directions:

INDICATIONS & USAGE SECTION

Directions:

Adults and children 2 years of age and older

Apply to painful muscles and joints. Genthly massage thoroughly into affected area.

Repeat as necessary but not more than 4 times daily.

Other infirmation:

STORAGE AND HANDLING SECTION

Other Information: Store in a cool dry place with lid closed tightly.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Aqueous (Deionozed filtered water) blend of certified * Organic Aloe Barbadensis Extract, Isopropyl Alcohol, *Ilex Paraguariensis Leaf Extract, Cinnamomum Camphora (camphor),Tocopheryl Acetate (Vitamin E Acetate), Carbomer, FDC Blue #1, FDCYellow #5, Methylparaben, Triethanolamine.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

30056-004-0430056-004-0430056-004-0330056-004-03

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
808955menthol 3.5 % Topical GelPSN7
808955menthol 0.035 MG/MG Topical GelSCD7
808955menthol 3.5 % Topical GelSY7

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
30056-004-03Elgin Pain Relief85 g in 1 BOTTLE, PUMPGEL857
30056-004-04Elgin Pain Relief113.4 g in 1 TUBEGEL113.47

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
30056-00430056-004-03, 30056-004-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
62025-01-16full-release2026-06-01 00:53:02

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 · 3 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Elgin Pain ReliefMENTHOLEco-Logics, Inc.375bfe83-c895-3ea7-e054-00144ff88e882025-10-18WarningsExact identifier
ndc (package): 30056-004-03
ndc (package): 30056-004-04
ndc (product): 30056-004
ndc11 (package): 30056000404
ndc11 (package): 30056000403
spl id: 4177d9fc-4fcc-4b80-e063-6294a90ad600
spl set id: 375bfe83-c895-3ea7-e054-00144ff88e88
Elgin Pain ReliefMENTHOLEco-Logics, Inc.378d1109-6511-1f63-e054-00144ff88e882025-10-18WarningsExact identifier
ndc (product): 30056-004
Elgin Pain ReliefMENTHOLEco-Logics, Inc.70eda21e-e566-42f4-9a49-b0d3ad0006522025-01-16WarningsExact identifier
ndc (product): 30056-004

Reported adverse events (FAERS/openFDA)#

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