FDA.reportPublic FDA data

EMUAID ® Pain Relief Cream

Manufacturer
Speer Laboratories LLC | Ariel Laboratories LP
Effective date
2025-02-25
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 20:41:01

Label at a glance#

ProductEMUAID Pain Relief
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

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, Glycerin, Potassium Cetyl Phosphate, Cetyl Alcohol, Helianthus Annuus (Sunflower) Seed Wax, Ethyl Macadamiate, Butyrospermum Parkii (Shea) Butter, Mentha Piperita Oil, Lavendula Officinalis (Lavender) Oil, Tocopherol, Sodium Benzoate, Sodium Levulinate, Allantoin, Arnica Montana Flower Extract, Carrageenan, Eugenia Caryophyllata (Clove) Oil, Gaultheria Precumbens (Wintergreen) Leaf Oil, Chammomilla Recutita Flower Extract, Camellia Sinensis (White Tea) Leaf Extract, Calophyllum Inophyllum Seed (Tamanu) Oil, Borago Officinalis Extract, Boswellia Serrata Resin Extract, Juniperus Communis (Juniper) Oil, Simmondsia Chinensis (Jojoba) Seed Oil.

SPL UNCLASSIFIED SECTION

Distributed by
SPEER Laboratories
Fort Lauderdale,
Florida 33309

PRINCIPAL DISPLAY PANEL - 120 g Tube Box

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC# 55926-0028-1

FOR ACHING MUSCLES & JOINTS

emuaid®

Pain Relief
Cream
2% MENTHOL

Natural,
Non-Steroidal

Deep Penetrating
EMUTANEOUS®
Transdermal
Delivery
Technology

Anti-Inflammatory,
Cooling Therapy

INTENSIVE PAIN RELIEF

4 oz (120g)

PRINCIPAL DISPLAY PANEL - 120 g Tube Box
PRINCIPAL DISPLAY PANEL - 120 g Tube Box

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
55926-0028-12025-02-26C16284748780-11030e365-4847-111a-e063-dadaa90a10e2EMUAID ® Pain Relief Cream
55926-0028-12024-07-30C16284748780-11030e365-4847-111a-e063-dadaa90a10e2EMUAID ® Pain Relief Cream
55926-0028-12024-01-30C16284748780-11030e365-4847-111a-e063-dadaa90a10e2EMUAID ® Pain Relief Cream

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55926-0028EMUAID PAIN RELIEF (MENTHOL) CREAM [SPEER LABORATORIES LLC]2Unmatched20250228_cd88de9e-1abf-40d2-ba7b-67e70dcc5fef.zip

Products#

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

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55926-002855926-0028-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 26 matching rows.

Name, UNII, Kind table
NameUNIIKind
MENTHOL, UNSPECIFIED FORML7T10EIP3AACTIB
WATER059QF0KO0RIACT
EMU OIL344821WD61IACT
GLYCERINPDC6A3C0OXIACT
POTASSIUM CETYL PHOSPHATE03KCY6P7UTIACT
CETYL ALCOHOL936JST6JCNIACT
HELIANTHUS ANNUUS SEED WAX42DG15CHXVIACT
ETHYL MACADAMIATEANA2NCS6V1IACT
SHEA BUTTERK49155WL9YIACT
PEPPERMINT OILAV092KU4JHIACT
LAVENDER OILZBP1YXW0H8IACT
TOCOPHEROLR0ZB2556P8IACT
SODIUM BENZOATEOJ245FE5EUIACT
SODIUM LEVULINATEVK44E1MQU8IACT
ALLANTOIN344S277G0ZIACT
ARNICA MONTANA FLOWEROZ0E5Y15PZIACT
CARRAGEENAN5C69YCD2YJIACT
CLOVE OIL578389D6D0IACT
METHYL SALICYLATELAV5U5022YIACT
CHAMOMILEFGL3685T2XIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
TAMANU OILJT3LVK84A1IACT
BORAGEPB618V0K2WIACT
INDIAN FRANKINCENSE4PW41QCO2MIACT
JUNIPER BERRY OILSZH16H44UYIACT
JOJOBA OIL724GKU717MIACT

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
d5b089b9-7e09-403b-9bd1-48abc21b4366cd88de9e-1abf-40d2-ba7b-67e70dcc5fef2025-02-25WarningsExact identifier
spl id: d5b089b9-7e09-403b-9bd1-48abc21b4366
spl set id: cd88de9e-1abf-40d2-ba7b-67e70dcc5fef

Reported adverse events (FAERS/openFDA)#

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