HEEL PAIN RELIEF ROLL-ON

Manufacturer
Guangzhou Liuquanmiao Import & Export Trade Co., Ltd.
Effective date
2026-03-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:48:34

Label at a glance#

ProductHEEL PAIN RELIEF ROLL-ON
Active ingredientLIDOCAINE, MENTHOL
Label structure15 sections

Dosage and administration

Adults and Children above 12 years old : · apply a thin layer to affected area every 6 to 8 hours, not more than 3 to 4 times daily · massage until thoroughly absorbed into skin · wash hands thoroughly with soap and water after each use · children under 12 years of age : ask a doctor

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4.0% ...... Purpose: Topical Anesthetic

Menthol 1.0% ...... Purpose: Topical Analgesic

Purpose

OTC - PURPOSE SECTION

(Lidocaine) Topical Anesthetic

(Menthol) Topical Analgesic

Use

INDICATIONS & USAGE SECTION

Temporarily relieves muscle soreness and minor joint pains in the wrist, knees, back, neck, hips, shoulders, elbows.

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

· on wounds or on irritated or damaged skin

· with a heating pad or device

· with other ointments, creams, sprays, or liniments

· if your are allergic to any ingredients of this product

When using this product

OTC - WHEN USING SECTION

· use only as directed

· avoid contact with the eyes, mucous membranes, or rashes

· do not bandage tightly

· do not expose the area to local heat or to direct sunlight

Stop use if

OTC - STOP USE SECTION

· skin reactions such as redness, swelling, blistering or other discomfort occur

· condition worsens or symptoms persist for more than 7 days

· symptoms clear up and occur again within a few days

· redness is present or excessive skin irritation occurs

Ask a doctor if

OTC - ASK DOCTOR SECTION

· skin reactions such as redness, swelling, blistering or other discomfort occur

· condition worsens or symptoms persist for more than 7 days

· symptoms clear up and occur again within a few days

· redness is present or excessive skin irritation occurs

If pregnant or breast-feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

Ask a health professional before use

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed accidentally , get medical help or contact with Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and Children above 12 years old:

· apply a thin layer to affected area every 6 to 8 hours, not more than 3 to 4 times daily

· massage until thoroughly absorbed into skin

· wash hands thoroughly with soap and water after each use

· children under 12 years of age: ask a doctor

Other Information

OTHER SAFETY INFORMATION

·Store at 20°C to 25°C (68°F - 77°F)

·Store in a cool dry place away from direct sunlight

Inactive Ingredients

INACTIVE INGREDIENT SECTION

.ALPHA.-TOCOPHEROL, D-, Aloe Vera Extract, Carbomer, Isopropyl myristate, Lavender Oil, Phenoxyethanol, Polysorbate 80, Propylene Glycol, Tartaric acid, Water

Questions or Comments

OTC - QUESTIONS SECTION

supports@povihomeofficial.com

83602-373

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

bottlebottleboxbox

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1804176lidocaine 4 % / menthol 1 % Topical GelPSN1
1804176lidocaine 0.04 MG/MG / menthol 0.01 MG/MG Topical GelSCD1
1804176lidocaine 4 % / menthol 1 % Topical GelSY1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
LIDOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-136942488015241GTIN-13: 6942488015241
EAN-13: 6942488015241
GTIN storage (14 digits): 06942488015241
BOX.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
070fbed5-7088-434a-a7ce-f2a64d8d40acProduct name220260107
bee66ce1-adb7-9d3b-67d9-582e4c54e80fProduct name520250819
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
eaba870a-6a9d-442e-8643-87b3f558a451Product name120250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
7d755fa1-1087-4dcd-98f0-6d4bba479a57Product name320210602
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
aed701d5-9c75-dfaf-7154-cde46179faeaProduct name920200313
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
332d03e4-aa24-4b11-841a-02bf41081920Product name120171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
68ed98f8-24c2-44a0-944a-6d36e82ce25aProduct name120141222
1cd42bc2-a430-c72b-636d-991b235fbf80Product name120140508
49fa150c-f0de-cce7-3d9c-993ed81c5698Product name120140508
4d7ae718-ed00-bae8-2abe-9eaec1eef7ffProduct name120140508
9137811f-f279-8640-5aeb-99fa2145d64dProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83602-373-73HEEL PAIN RELIEF ROLL-ON1 in 1 BOXGEL11
83602-373-73HEEL PAIN RELIEF ROLL-ON73 mL in 1 BOTTLEGEL731

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83602-37383602-373-73

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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
HEEL PAIN RELIEF ROLL-ONLIDOCAINE AND MENTHOLGuangzhou Liuquanmiao Import & Export Trade Co., Ltd.4c06c4a4-557b-8bb1-e063-6294a90a91252026-03-02WarningsExact identifier
ndc (package): 83602-373-73
ndc (product): 83602-373
ndc11 (package): 83602037373
spl id: 4c06c493-dd13-9e4e-e063-6294a90abef3
spl set id: 4c06c4a4-557b-8bb1-e063-6294a90a9125

Reported adverse events (FAERS/openFDA)#

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