EXTRA STRENGTH eez-away

Manufacturer
EEZAWAY RELIEF INC
Effective date
2019-04-03
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 22:59:05

Label at a glance#

ProductEXTRA STRENGTH eez-away
Active ingredientMENTHOL, UNSPECIFIED FORM
Label structure8 sections

Indications and uses

temporarily relieves minor pain associated with: ■ arthritis ■ simple backache ■ muscle strains ■ sprains ■ bruises ■ cramps

Dosage and administration

adults and children over 12 years : ■ apply generously to affected area ■ massage into painful area until thoroughly absorbed into skin ■ repeat as necessary, but no more than 3 to 4 times daily ■ IF MEDICINE COMES IN CONTACT WITH HANDS, WASH WITH SOAP AND WATER children 12 years or younger: ask 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

temporarily relieves minor pain associated with: ■ arthritis ■ simple backache ■ muscle strains ■ sprains ■ bruises ■ cramps

Warnings

WARNINGS SECTION

For external use only

When using this product ■ use only as directed ■ do not bandage tightly or use with heating pad ■ avoid contact with eyes and mucous
membranes ■ do not apply to wounds or damaged, broken or irritated skin ■ a transient burning sensation or redness may occur upon
application but generally disappears in several days ■ if severe burning sensation occurs, discontinue use immediately ■ do not
expose the area treated with product to heat or direct sunlight

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

Flammable ■ keep away from fire or flame

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

adults and children over 12 years: ■ apply generously to affected area ■ massage into painful area until thoroughly absorbed into skin
■ repeat as necessary, but no more than 3 to 4 times daily
■ IF MEDICINE COMES IN CONTACT WITH HANDS, WASH WITH SOAP AND WATER
children 12 years or younger: ask a doctor

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Emu Oil, Fragrance, Glucam P-20, Isopropyl Alcohol USP, Oleth-10, PEG-75 Lanolin, Purified Water, Sodium Thiosulfate Pentahydrate Crystal USP, Tincture of Iodine USP

SPL UNCLASSIFIED SECTION

FOR TEMPORARY RELIEF OF MINOR ACHES AND PAINS ASSOCIATED WITH

• ARTHRITIS
• ACUTE BACKACHE
• SORE & TIRED MUSCLES

Recommended by

Physicians • Professionals • Atheletic Trainers

For Topical Use Only

BLUE PLANT FARMS

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

eez-labeleez-label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
884802menthol 2.5 % Topical SolutionPSN3
884802menthol 25 MG/ML Topical SolutionSCD3
884802menthol 2.5 % Topical SolutionSY3

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
69678-131-022021-01-29C16284748780-1ba0f9c33-4e17-a910-e053-dadaa90a0b85EXTRA STRENGTH eez-away

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69678-131-02EXTRA STRENGTH eez-away88 mL in 1 BOTTLELIQUID883

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69678-131EXTRA STRENGTH EEZ-AWAY (MENTHOL) LIQUID [EEZAWAY RELIEF INC]3Legacy NDC, 1 package rows20190404_9d7fb7ea-a7f1-4c2b-8e38-ed876a72a93a.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69678-13169678-131-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
761a7769-871b-4f50-a9d4-3a9823cf91329d7fb7ea-a7f1-4c2b-8e38-ed876a72a93a2019-04-03WarningsExact identifier
spl id: 761a7769-871b-4f50-a9d4-3a9823cf9132
spl set id: 9d7fb7ea-a7f1-4c2b-8e38-ed876a72a93a

Reported adverse events (FAERS/openFDA)#

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