Rapid Relief

Manufacturer
RAPID AID VIET NAM COMPANY LIMITED
Effective date
2025-11-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:43:46

Label at a glance#

ProductRapid Relief
Active ingredientLIDOCAINE, MENTHOL
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 to the skin Apply 1 patch at a time to the affected area, not more than 3 times daily. Remove patch from the skin. Do not leave on skin for more than a total of 8 hours per day Children under 12 years of age: Do not use, consult a physician. Supervise children when they use this product

Storage and handling

Store between 15-30℃(59-86℉) keep away from children

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4 % +Menthol 1% w/w.

Purpose

OTC - PURPOSE SECTION

Lidocaine: Topical anesthetic / Menthol: Topical analgesic

Use

INDICATIONS & USAGE SECTION

For the temporary relief of minor 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

When using this product:

OTC - WHEN USING SECTION

Use only as directed

Do not bandage tightly

Avoid contact with eyes, mucous membranes or rashes

If contact occurs, rinse thoroughly with water

Stop use and ask a doctor if:

OTC - ASK DOCTOR SECTION

Localized skin reactions occur, such as rash, itching, redness, irritation, pain, swelling and blistering

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 health professional before 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 to the skin

Apply 1 patch at a time to the affected area, not more than 3 times daily.

Remove patch from the skin.

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

Children under 12 years of age:

Do not use, consult a physician.

Supervise children when they use this product

STORAGE AND HANDLING

STORAGE AND HANDLING SECTION

Store between 15-30℃(59-86℉) keep away from children

Inactive ingredients

INACTIVE INGREDIENT SECTION

Acryloyldime/ Sodium Acryloyldimethyltaurate copolymer, Dihydroxyaluminum aminoacetetel, 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 PatchPSN2
1249758lidocaine 0.04 MG/MG / menthol 0.01 MG/MG Medicated PatchSCD2
1249758lidocaine 4 % / menthol 1 % Medicated PatchSY2

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
83569-016-06Rapid Relief600 g in 1 POUCHPATCH6002
83569-016-06Rapid Relief1 in 1 BOXPATCH12

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83569-01683569-016-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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 ReliefPAIN RELIEF PATCH LIDOCAINE 4% MENTHOL 1%RAPID AID VIET NAM COMPANY LIMITED43616ad7-58bb-e5ad-e063-6394a90a192b2025-11-13WarningsExact identifier
ndc (package): 83569-016-06
ndc (product): 83569-016
ndc11 (package): 83569001606
spl id: 43765133-002c-6449-e063-6394a90a901c
spl set id: 43616ad7-58bb-e5ad-e063-6394a90a192b
Rapid ReliefPAIN RELIEF PATCH LIDOCAINE 4% MENTHOL 1%RAPID AID VIET NAM COMPANY LIMITED434df0be-49ff-aa56-e063-6394a90a3b5a2025-11-11WarningsExact identifier
ndc (product): 83569-016

Reported adverse events (FAERS/openFDA)#

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