FDA.reportPublic FDA data

eez-away Pain Relief

Manufacturer
EEZAWAY RELIEF INC
Effective date
2018-11-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:57:13

Label at a glance#

Producteez-away Pain Relief
Active ingredientMENTHOL, UNSPECIFIED FORM
Label structure10 sections

Indications and uses

for temporary relief of minor aches and pains of muscles and joints associated with • bruises • sprains • arthritis • strains

Dosage and administration

• adults and children 12 years of age and older: apply to affected area no more than 10 times a day as needed for pain. • children under 12 years of age: do not use, consult a doctor.

Label contents#

Full prescribing information#

Active ingredient:

OTC - ACTIVE INGREDIENT SECTION

Menthol 2.50%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

for temporary relief of minor aches and pains of muscles and joints associated with • bruises • sprains • arthritis • strains

Warnings:

WARNINGS SECTION

For external use only

When using this product  

Do not bandage tightly • avoid contact with eyes • do not apply to wounds or damaged skin • do not use with heating pads or other heating devices.

Stop use and ask a doctor if

• Condition worsens or if 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 10 times a day as needed for pain.

• children under 12 years of age: do not use, consult a doctor.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Isopropyl Alcohol, Deionized Water, PEG-75 Lanolin, Oleth-10, PPG-20 Methyl Glucose Ether, Iodine, Sodium Iodide, Ethyl Alcohol, Sodium Thiosulfate Pentahydrate, Fragrance.

OTC - QUESTIONS SECTION

To reorder call:

1-877 600 0016

SPL UNCLASSIFIED SECTION

NEW! EXTRA STRENGTH ROLL-ON

Recommended by

  • Top Physicians
  • Professional Athletes
  • Trainers

Distributed exclusively by

eez-Away Inc. P.O. Box 161, Hunterville, NC 28070

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

eez-labeleez-label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5f30b278-5791-4113-8781-878a9221ef8aProduct name220230125
2a70c781-a755-4d76-b20a-a958acfbdcdcProduct name220190619
304592ef-4a8a-4c22-8e8c-af73aa3d60e5Product name120180703
ac0821a1-ce75-4ea7-880a-59eecaecdf22Product name120180703
db5dc4f9-b907-46f6-8fb7-babcf04bbe5cProduct name120180619
4073022c-5d5d-48f5-82ed-091ad146a4b2Product name120171211
41e9d6cf-3ed7-4c44-a57e-0685058d0896Product name120170824
5e652c92-68fd-426b-b0e7-5fc64e0b9f99Product name120170309
9ffbd0ae-0bce-c086-b707-f0da5f8cd7c5Product name120150828
ddc0c11a-bba8-408f-b3c7-c4828b4bcc8cProduct name120150421

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69678-111-022020-01-31C16284748780-19d75b9d0-bc71-f424-e053-dadaa90a57ceeez-away Pain Relief

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69678-111-02eez-away Pain Relief84 mL in 1 BOTTLELIQUID842

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69678-111EEZ-AWAY PAIN RELIEF (MENTHOL) LIQUID [EEZAWAY RELIEF INC]2Legacy NDC, 1 package rows20181110_da36730e-a684-4ba7-9d4d-013aceceb98b.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69678-11169678-111-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
MENTHOL, UNSPECIFIED FORML7T10EIP3AACTIB
ISOPROPYL ALCOHOLND2M416302IACT
WATER059QF0KO0RIACT
PEG-75 LANOLIN09179OX7TBIACT
POLYOXYL-10 OLEYL ETHERJD797EF70JIACT
PPG-20 METHYL GLUCOSE ETHER3WV1T97D3KIACT
IODINE9679TC07X4IACT
SODIUM IODIDEF5WR8N145CIACT
ALCOHOL3K9958V90MIACT
SODIUM THIOSULFATEHX1032V43MIACT

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
6e3a325c-9a58-4514-8478-c9f5858cc32cda36730e-a684-4ba7-9d4d-013aceceb98b2018-11-09WarningsExact identifier
spl id: 6e3a325c-9a58-4514-8478-c9f5858cc32c
spl set id: da36730e-a684-4ba7-9d4d-013aceceb98b

Reported adverse events (FAERS/openFDA)#

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