JOIYA Ease Topical Pain Relieving Gel

Manufacturer
Prime Enterprises
Effective date
2020-06-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:27:29

Label at a glance#

ProductJOIYA Ease
Active ingredientMENTHOL, LIDOCAINE HYDROCHLORIDE
Label structure9 sections

Dosage and administration

Adults and children over 12 years: Apply a thin layer to affected area every 6 to 8 hours, but no more than 3 to 4 times a daily If product comes into contact with hands, wash hands with soap and water Children 12 years or younger ask a doctor

Label contents#

Full prescribing information#

Use

INDICATIONS & USAGE SECTION

Temporarily relieves minor pain

Warnings

WARNINGS SECTION

For external use only

Do not use on large areas of the body or on cut, irratated or swollen skin, on puncture wounds; for more than one week with out consulting a doctor

Stop use and ask a doctor if condition worsens irratation develops redness appears symptoms persist for more than 7 days or clear up and occurs again with a few days

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 product is swallowed get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children over 12 years:

  • Apply a thin layer to affected area every 6 to 8 hours, but no more than 3 to 4 times a daily
  • If product comes into contact with hands, wash hands with soap and water
  • Children 12 years or younger ask a doctor

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Lidocaine Hydrochloride 4%

Menthol 15%

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aesculus Hippocastanum (Horse Chestnut) Seed Extract, Arnica Montana Flower Extract, Borago Officinalis Seed Oil, Camellia Oleifera (Green Tea) Leaf Extract, Cannabidiol, Capsicum Frutescens Resin, Chamomilla Recutita (Matricaria) Flower Extract, Curcuma Longa (Turmeric) Root Extract, Dimethyl Isosorbide, Glycerin, Mentha Piperita (Peppermint) Oil, Polyacrylate-13, Polyisobutene, Polysorbate 20, SD Alcohol 40-B, Sodium Hydroxide, Water​

Questions and comments

OTC - QUESTIONS SECTION

1 (800) 955-4173

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Packaging Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display LabelPrincipal Display Label

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58443-033658443-0336-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 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
e77aebf1-31f8-a318-e053-2a95a90ae148a6a77142-4bec-1be9-e053-2995a90ab1482022-08-30WarningsExact identifier
spl set id: a6a77142-4bec-1be9-e053-2995a90ab148

Reported adverse events (FAERS/openFDA)#

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