83559-018

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 05:10:18

Label at a glance#

ProductENOKON PAIN RELIEF Spray.
Active ingredientLIDOCAINE
Label structure14 sections

Dosage and administration

adults and children over 12 years: *spray affected area every 6 to 8 hours, not to exceed 3 applications in a 24-hour period *product will dry quickly on its own, and does not need to be rubbed in 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 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

*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 label
*do not allow contact with the eyes and mucous membranes
*avoid spraying on face
*avoid inhalation of spray
*do not bandage or apply local heat (such as heating pads) or a medicated patch to 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:
*spray affected area every 6 to 8 hours, not to exceed 3 applications in a 24-hour period
*product will dry quickly on its own, and does not need to be rubbed in
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

light mineral oil, methylparaben sodium, peg-32 monostearate, peg-6 monostearate, sorbic acid, stearyl alcohol, water

Questions

OTC - QUESTIONS SECTION

Questions or comments?

Call 1 858 905 0218

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1122

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-136974159743962GTIN-13: 6974159743962
EAN-13: 6974159743962
GTIN storage (14 digits): 06974159743962
30g.jpg
BarcodeEAN-136974159743979GTIN-13: 6974159743979
EAN-13: 6974159743979
GTIN storage (14 digits): 06974159743979
50g.jpg

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83559-01883559-018-01, 83559-018-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
ENOKON PAIN RELIEF Spray.PAIN RELIEF SPRAY.Henan Enokon Medical Instrument Co., Ltd.5675ec21-b947-2206-e063-6294a90aa5092026-07-12WarningsExact identifier
ndc (package): 83559-018-02
ndc (package): 83559-018-01
ndc (product): 83559-018
ndc11 (package): 83559001801
ndc11 (package): 83559001802
spl id: 5675ec21-b948-2206-e063-6294a90aa509
spl set id: 5675ec21-b947-2206-e063-6294a90aa509

Reported adverse events (FAERS/openFDA)#

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