FDA.reportPublic FDA data

EMUAID ® Pain Relieving Cream

Manufacturer
Speer Laboratories LLC | Ariel Laboratories LP
Effective date
2023-06-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:55:39

Label at a glance#

ProductEMUAID Pain Relieving
Active ingredientMenthol, Unspecified Form
Label structure9 sections

Indications and uses

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

Dosage and administration

Adults and children 12 yrs. of age and older, apply to affected area not more than 3 to 4 times daily. Children under 12 years of age: consult a doctor.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Menthol 2%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

for temporary relief of minor aches and pains of muscles and joints associated with

  • simple backache
  • bruises
  • sprains
  • arthritis
  • strains

Warnings

WARNINGS SECTION

OTC - WHEN USING SECTION

For external use only. When using this product

  • Do not bandage tightly
  • Avoid contact with the eyes
  • Do not apply to wounds or damaged skin
  • Do not use a heating pad or other heating devices

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • Condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding, 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 12 yrs. of age and older, apply to affected area not more than 3 to 4 times daily.
  • Children under 12 years of age: consult a doctor.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Emu Oil/Hemp Extract, Glycerin, Potassium Cetyl Phosphate, Rhus Verniciflua Peel Cera (Berry Wax), Glyceryl Stearate, Ethyl Macadamiate, Arnica Montana Flower Extract, Butyrospermum Parkii (Shea) Butter, Cetearyl Olivate, Polysorbate 60, Sorbitan Olivate, Mentha Piperita Oil, Tocopherol, Lavendula Officinalis (Lavender) Oil, Sodium Benzoate, Sodium Levulinate, Juniperus Communis (Juniper) Oil, Allantoin, Calophyllum Inophyllum Seed Oil, Borago Officinalis Extract, Boswellia Serrata Resin Extract, Carrageenan, Simmondsia Chinensis (Jojoba) Seed Oil, Sodium Hydroxide, Eugenia Caryophyllata (Clove) Oil, Gaultheria Procumbens (Wintergreen) Leaf Extract, Camellia Sinensis (White Tea) Leaf Extract, Chamomilla Recutita Flower Extract.

SPL UNCLASSIFIED SECTION

Distributed by
SPEER Laboratories
Fort Lauderdale,
Florida 33309

PRINCIPAL DISPLAY PANEL - 120 G Tube Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INTENSIVE PAIN RELIEF

emuaid®

Pain Relieving Cream
2% MENTHOL

  • ADVANCED RECOVERY FOR
    ACHING MUSCLES & JOINTS
  • DEEP PENETRATING WITH
    HEMP INFUSED EMU OIL
  • COOLING THERAPY
    FOR INSTANT RELIEF
  • NATURAL, NON-GREASY,
    SOOTHING FORMULA

ESSENTIAL OILS
LAB TESTED
PARABEN FREE

4 OZ / 120 G

PRINCIPAL DISPLAY PANEL - 120 G Tube Label
PRINCIPAL DISPLAY PANEL - 120 G Tube Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
55926-0026-12024-07-30C16284748780-11030e365-6d68-111a-e063-dadaa90a10e2EMUAID ® Pain Relieving Cream
55926-0026-12024-01-30C16284748780-11030e365-6d68-111a-e063-dadaa90a10e2EMUAID ® Pain Relieving Cream

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55926-0026-1EMUAID Pain Relieving120 g in 1 TUBECREAM1201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55926-0026EMUAID PAIN RELIEVING (MENTHOL, UNSPECIFIED FORM) CREAM [SPEER LABORATORIES LLC]11 package rows20230718_9f387a47-b6a2-41a1-a21f-1bd4c281fc0a.zip

Products#

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

DailyMed product names page 1 of 1 · 32 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55926-002655926-0026-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 31 matching rows.

Name, UNII, Kind table
NameUNIIKind
Menthol, Unspecified FormL7T10EIP3AACTIB
Water059QF0KO0RIACT
Emu Oil344821WD61IACT
CANNABIS SATIVA FLOWERING TOP8X454SZ22DIACT
GlycerinPDC6A3C0OXIACT
Potassium Cetyl Phosphate03KCY6P7UTIACT
TOXICODENDRON VERNICIFLUUM FRUIT RIND WAX6RG2461FCHIACT
Glyceryl Monostearate230OU9XXE4IACT
Ethyl MacadamiateANA2NCS6V1IACT
Arnica Montana FlowerOZ0E5Y15PZIACT
SHEA BUTTERK49155WL9YIACT
Cetearyl Olivate58B69Q84JOIACT
Polysorbate 60CAL22UVI4MIACT
Sorbitan OlivateMDL271E3GRIACT
Peppermint OilAV092KU4JHIACT
TocopherolR0ZB2556P8IACT
LAVENDER OILZBP1YXW0H8IACT
Sodium BenzoateOJ245FE5EUIACT
Sodium LevulinateVK44E1MQU8IACT
JUNIPER BERRY OILSZH16H44UYIACT
Allantoin344S277G0ZIACT
Tamanu OilJT3LVK84A1IACT
BORAGEPB618V0K2WIACT
INDIAN FRANKINCENSE4PW41QCO2MIACT
Carrageenan5C69YCD2YJIACT
Jojoba Oil724GKU717MIACT
Sodium Hydroxide55X04QC32IIACT
CLOVE OIL578389D6D0IACT
Gaultheria Procumbens Leaf2125M16OWNIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
CHAMOMILEFGL3685T2XIACT

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
1b832911-da07-4a6a-9a23-a269dee0bf259f387a47-b6a2-41a1-a21f-1bd4c281fc0a2023-06-23WarningsExact identifier
spl id: 1b832911-da07-4a6a-9a23-a269dee0bf25
spl set id: 9f387a47-b6a2-41a1-a21f-1bd4c281fc0a

Reported adverse events (FAERS/openFDA)#

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