FOOT PAIN RELIEF ROLL-ON

Manufacturer
Guangzhou Zhupuyou E-commerce Co., Ltd | Shanghai Chuangshi Medical Technology (Group) Co., Ltd.
Effective date
2025-11-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:16:55

Label at a glance#

ProductFOOT PAIN RELIEF ROLL-ON
Active ingredientLIDOCAINE, MENTHOL
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4%
Menthol 1%

OTC - PURPOSE SECTION

Topical Analgesic

INDICATIONS & USAGE SECTION

Temporarily relieves muscle soreness and minorjoint pains in the wrist, knees, back, neck, hipsshoulders,elbows.

WARNINGS SECTION

For external use only

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 thisproduct

OTC - WHEN USING SECTION


use only as directed
avoid contact with the eyes, mucousmembranes, or rashes
do not bandage tightly
do not expose the area to local heat or to direct sunlight

OTC - STOP USE SECTION


skin reactions such as redness, swelling,blistering or other discomfort occur
condition worsens or symptoms persist formore than 7 days
symptoms clear up and occur again within afew days
redness is present or excessive skin irritation occurs

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

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

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
252967lidocaine 4 % / menthol 1 % Topical SolutionPSN1
252967lidocaine 40 MG/ML / menthol 10 MG/ML Topical SolutionSCD1

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-136942488005938GTIN-13: 6942488005938
EAN-13: 6942488005938
GTIN storage (14 digits): 06942488005938
label.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
84165-017-01FOOT PAIN RELIEF ROLL-ON1 in 1 BOXLIQUID11
84165-017-01FOOT PAIN RELIEF ROLL-ON73 mL in 1 BOTTLELIQUID731
84165-017-02FOOT PAIN RELIEF ROLL-ON2 in 1 BOXLIQUID21
84165-017-02FOOT PAIN RELIEF ROLL-ON73 mL in 1 BOTTLELIQUID731
84165-017-03FOOT PAIN RELIEF ROLL-ON3 in 1 BOXLIQUID31
84165-017-03FOOT PAIN RELIEF ROLL-ON73 mL in 1 BOTTLELIQUID731
84165-017-04FOOT PAIN RELIEF ROLL-ON4 in 1 BOXLIQUID41
84165-017-04FOOT PAIN RELIEF ROLL-ON73 mL in 1 BOTTLELIQUID731
84165-017-05FOOT PAIN RELIEF ROLL-ON5 in 1 BOXLIQUID51
84165-017-05FOOT PAIN RELIEF ROLL-ON73 mL in 1 BOTTLELIQUID731
84165-017-06FOOT PAIN RELIEF ROLL-ON6 in 1 BOXLIQUID61
84165-017-06FOOT PAIN RELIEF ROLL-ON73 mL in 1 BOTTLELIQUID731
84165-017-07FOOT PAIN RELIEF ROLL-ON7 in 1 BOXLIQUID71
84165-017-07FOOT PAIN RELIEF ROLL-ON73 mL in 1 BOTTLELIQUID731
84165-017-08FOOT PAIN RELIEF ROLL-ON73 mL in 1 BOTTLELIQUID731
84165-017-08FOOT PAIN RELIEF ROLL-ON8 in 1 BOXLIQUID81
84165-017-09FOOT PAIN RELIEF ROLL-ON9 in 1 BOXLIQUID91
84165-017-09FOOT PAIN RELIEF ROLL-ON73 mL in 1 BOTTLELIQUID731
84165-017-10FOOT PAIN RELIEF ROLL-ON10 in 1 BOXLIQUID101
84165-017-10FOOT PAIN RELIEF ROLL-ON73 mL in 1 BOTTLELIQUID731

Products#

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

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

NDC Codes#

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
FOOT PAIN RELIEF ROLL-ONLIDOCAINE, MENTHOLGuangzhou Zhupuyou E-commerce Co., Ltd43edcea0-ab04-f368-e063-6294a90a817a2025-11-19WarningsExact identifier
ndc (package): 84165-017-08
ndc (package): 84165-017-02
ndc (package): 84165-017-01
ndc (package): 84165-017-03
ndc (package): 84165-017-05
ndc (package): 84165-017-06
ndc (package): 84165-017-07
ndc (package): 84165-017-09
ndc (package): 84165-017-10
ndc (package): 84165-017-04
ndc (product): 84165-017
ndc11 (package): 84165001703
ndc11 (package): 84165001702
ndc11 (package): 84165001707
ndc11 (package): 84165001704
ndc11 (package): 84165001710
ndc11 (package): 84165001708
ndc11 (package): 84165001706
ndc11 (package): 84165001705
ndc11 (package): 84165001701
ndc11 (package): 84165001709
spl id: 43edcea0-ab05-f368-e063-6294a90a817a
spl set id: 43edcea0-ab04-f368-e063-6294a90a817a

Reported adverse events (FAERS/openFDA)#

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