83559-017

Manufacturer
Henan Enokon Medical Instrument Co., Ltd.
Effective date
2026-07-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-07-18 05:10:16

Label at a glance#

ProductENOKON PAIN RELIEF Cream
Active ingredientLIDOCAINE
Label structure14 sections

Dosage and administration

*Adults and children over 12 years: Apply a thin layer to affected area every 6 to 8 hours, not to exceed 3 applications in a 24-hour period, massage into painful area until thoroughly absorbed into skin *Children 12 years or younger: ask a doctor

Storage and handling

Store at controlled room temperature 68°–77°F (20°–25°C)

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

LIDOCAINE HYDROCHLORIDE 4%

Purpose

OTC - PURPOSE SECTION

TOPICAL ANESTHETIC

Use

INDICATIONS & USAGE SECTION

temporarily relieves minor pain

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

*if you have serious foot problems, such as ulcers or infections, on large areas of the body or on cut, irritated or swollen skin on puncture wounds
*for more than one week without consulting a doctor

When Using

OTC - WHEN USING SECTION

*use only as directed, read and follow all directions and warnings on this carton.
*do not allow contact with the eyes and mucus membranes
*do not bandage tightly or apply local heat (such as heating pads) or a medicated patch to the area of use
*do not use at the same time as other topical analgesics

Stop Use

OTC - STOP USE SECTION

*condition worsens
*redness is present
*irritation develops
*symptoms persist for more than 7 days or clear up and occur again within a few days

Ask Doctor

OTC - ASK DOCTOR SECTION

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

If 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, not to exceed 3 applications in a 24-hour period, massage into painful area until thoroughly absorbed into skin
*Children 12 years or younger: ask a doctor

Other information

STORAGE AND HANDLING SECTION

Store at controlled room temperature 68°–77°F (20°–25°C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

pegoxol-7 stearate, cetyl alcohol, light mineral oil, ethylparaben, water

Questions

OTC - QUESTIONS SECTION

Questions or comments?

Call 1 858 905 0218

​PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1122

Products#

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DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83559-01783559-017-01, 83559-017-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
567502df-d5f1-a3f7-e063-6394a90a57f0567502df-d5f0-a3f7-e063-6394a90a57f02026-07-12WarningsExact identifier
spl id: 567502df-d5f1-a3f7-e063-6394a90a57f0
spl set id: 567502df-d5f0-a3f7-e063-6394a90a57f0

Reported adverse events (FAERS/openFDA)#

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