Rapid Relief

Manufacturer
RAPID AID VIET NAM COMPANY LIMITED
Effective date
2025-11-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:43:32

Label at a glance#

ProductRapid Relief
Active ingredientMENTHOL, LIDOCAINE
Label structure13 sections

Dosage and administration

Adults and children 12 years of age and older: Clean and dry affected area Remove film from patch and apply sticky side to desired area Apply patch to affected area not more than 3 times daily Do not leave on skin for more than a total of 8 hours per day Can be cut for custom sizing of pain area Children under 12 years of age: Do not use, consult a doctor Supervise children when 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% w/w.

Purpose

OTC - PURPOSE SECTION

Topical anesthetic

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 this may result in excessive skin irritation or skin burn
If you are allergic to any ingredients of this product
In large quantities, 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 eyes, mucous membranes or rashes.If contact occurs, rinse thoroughly

Do not bandage tightly

Do not use at the same time as other topical analgesics.

Stop use and ask a doctor if:

OTC - ASK DOCTOR SECTION

Localized skin reactions occur, such as rash, itching, redness, irritation, pain and blistering as rare but serious burns can occur

Condition worsens

Symptoms persist for more than 7 days

Symptoms clear up and occur again within a few days

If pregnant or breastfeeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding, ask a physicianbefore use.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. 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 film from patch and apply sticky side to desired area

Apply patch to affected area not more than 3 times daily

Do not leave on skin for more than a total of 8 hours per day

Can be cut for custom sizing of pain area

Children under 12 years of age:

Do not use, consult a doctor

Supervise children when 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,DMDM

hydantoin, Edetic acid, Glycerin, Laurocapram, Polyacrylic acid, Propylene glycol,Sodium polyacrylate,

Tartaric acid, Titanium dioxide,Water.

IMAGE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

IMAGEIMAGE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1249758lidocaine 4 % / menthol 1 % Medicated PatchPSN1
1249758lidocaine 0.04 MG/MG / menthol 0.01 MG/MG Medicated PatchSCD1
1249758lidocaine 4 % / menthol 1 % Medicated PatchSY1

DailyMed Pharmacologic Classes#

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

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
83569-014-01Rapid Relief100 g in 1 POUCHPATCH1001

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
83569-01483569-014-01

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

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 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Rapid ReliefPLANTAR FASCIITIS PAIN RELIEF LIDOCAINE 4% MENTHOL 1%RAPID AID VIET NAM COMPANY LIMITED434cb8b2-a996-5360-e063-6394a90ada032025-11-13WarningsExact identifier
ndc (product): 83569-014
Rapid ReliefPLANTAR FASCIITIS PAIN RELIEF LIDOCAINE 4% MENTHOL 1%RAPID AID VIET NAM COMPANY LIMITED4360e0d1-46cd-ab4b-e063-6394a90a55e12025-11-12WarningsExact identifier
ndc (package): 83569-014-01
ndc (product): 83569-014
ndc11 (package): 83569001401
spl id: 4360f33e-1470-ab4d-e063-6394a90a6816
spl set id: 4360e0d1-46cd-ab4b-e063-6394a90a55e1

Reported adverse events (FAERS/openFDA)#

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