Rapid Relief Hot Relief Patch

Manufacturer
RAPID AID VIET NAM CO., LTD
Effective date
2024-03-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:07:27

Label at a glance#

ProductRapid Relief Hot Relief Patch
Active ingredientCapsaicin
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 to 4 times daily.  Remove patch from the skin after at most 8-hour application. Children under 12 years of age: consult a doctor

Storage and handling

 Avoid storing product in direct sunlight  Protect product from excessive moisture

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Capsaicin 0.013 %

Purpose

OTC - PURPOSE SECTION

Topical analgesic

Use

INDICATIONS & USAGE SECTION

For temporary relief of minor pain associated with:
arthritis,
simple backache,
strains,
sprains,
bruises

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

 On wounds or damaged skin
With a heating pad

When using this product:

OTC - WHEN USING SECTION

 Use only as directed
 Do not bandage tightly
 Avoid contact with eyes, mucous membranes or rashes
 Discontinue use at least 1 hour before a bath or shower
 Do not use immediately after a bath or shower

Stop use and ask a doctor if:

OTC - STOP USE SECTION

 Condition worsens, Symptoms persist for more than 7 days or clear up and occur again within a few days.
 Redness is present or irritation or rash develops.
 A sever burning sensation occurs.

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.

If pregnant or breast feeding

PREGNANCY SECTION

ask a health professional before use.

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 to 4 times daily.
 Remove patch from the skin after at most 8-hour application.
Children under 12 years of age: consult a doctor

STORAGE AND HANDLING

STORAGE AND HANDLING SECTION

 Avoid storing product in direct sunlight
 Protect product from excessive moisture

Inactive ingredients

INACTIVE INGREDIENT SECTION

Acyclovir, Dihydroxyaluminum aminoacetetel, DMDM hydantoin, Edetate Disodium Anhydrous, Glycerin, Polyacrylic acid, Sodium polyacrylate, Sodium Acryloyldimethyltaurate-acrylamide copolymer, Tartaric acid, Titanium dioxide, Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83569-00483569-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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
1500b291-0acb-0b03-e063-6294a90ab4c3a0dfb51b-3993-4480-bd81-8ae2b0ffc4b52024-03-31WarningsExact identifier
spl set id: a0dfb51b-3993-4480-bd81-8ae2b0ffc4b5

Reported adverse events (FAERS/openFDA)#

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