Rapid Relief Plantar Fasciitis Pain Relief Patch

Manufacturer
RAPID AID VIET NAM CO., LTD
Effective date
2025-10-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
monthly-update
Hydrated at
2026-06-03 17:38:42

Label at a glance#

ProductRapid Relief Plantar Fasciitis Pain Relief Patch
Active ingredientMENTHOL, LIDOCAINE
Label structure12 sections

Dosage and administration

Adults and children 12 years of age and older:Clean and dry affected area · Remove flm from patch and apply sticky side to desired area · Apply patch toaffected area not more than 3 times daily. Do not leave on skin for more than a total of8 hours per day. Canbe cut for custom sizing of pain area . Children under 12 years of age: Consult a doctor . Supervise childrenwhen they use this product.

Storage and handling

Store between 15-30℃(59-86℉) 

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4% 
Menthol 1% 

Purpose

OTC - PURPOSE SECTION

Topical anesthetic

Topical analgesic

Use

INDICATIONS & USAGE SECTION

For temporary relief of pain.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

More than 1 patch at a time . On wounds or damaged skin . With a heating pad such as electric heating pad, as thismay result in excessive skin irritation or skin burn · lfyou are allergic to anyingredients of this product . ln largequantities, particularly over raw surfaces or blistered areas . More than one week without consulting a doctor.

When using this product:

OTC - WHEN USING SECTION

Use only as directed . Do not apply to wounds or damaged, broken, or irritated skin · Avoid contact with eyesmucous membranes or rashes. lf contact occurs, rinse thoroughly · Do not bandage tightly. Do not use at thesame time as other topical analgesics.

Stop use and ask a doctor if:

OTC - STOP USE SECTION

. Localized skin reactions occur, such as rash, itching, redness, irritation, pain and blistering as rare butserious burns can occur . Condition worsens · Symptoms persist for more than 7 days · Symptoms clear upand occur again within a few days.

If pregnant or breast feeding, ask a physician 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 12 years of age and older:Clean and dry affected area · Remove flm from patch and apply sticky side to desired area · Apply patch toaffected area not more than 3 times daily. Do not leave on skin for more than a total of8 hours per day. Canbe cut for custom sizing of pain area . Children under 12 years of age: Consult a doctor . Supervise childrenwhen they use this product.

STORAGE AND HANDLING

STORAGE AND HANDLING SECTION

Store between 15-30℃(59-86℉) 

Inactive ingredients

INACTIVE INGREDIENT SECTION

Acrylamide/Sodium acryloyldimethyltaurate copolymer, Dihydroxyaluminum aminoacetate, DMDMhydantoin, Edetic acid, Glycerin, Laurocapram, Polyacrylic acid, Propylene glycol, Sodium polyacrylateTartaric acid,Titanium dioxide. Water.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83569-00783569-007-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12025-07-10full-release2026-06-01 01:06:59

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
4ca4b09d-01c1-05f1-e063-6294a90a3590eccfbb3c-3f42-4e20-824e-233cd83a76732026-03-10WarningsExact identifier
spl set id: eccfbb3c-3f42-4e20-824e-233cd83a7673

Reported adverse events (FAERS/openFDA)#

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