RAPID RELIEF- pain relief patch patch

Rapid Relief by

Drug Labeling and Warnings

Rapid Relief by is a Otc medication manufactured, distributed, or labeled by RAPID AID VIET NAM COMPANY LIMITED. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Camphor 110mg +Menthol 33mg + Capsicum Extract 22mg

ask a doctor if：

Condition worsens,

Severe skin irritation occurs

Pain persist for more than 7 days

Symptoms clear up and occur again within a few days.

You experience pain, swelling or blistering, as rare but serious burns can occur

headache or redness occurs

NO NOT USE

do not get into eyes or on mucous membranes. If contact occurs, rinse thoroughly with water

do not apply to wounds, damaged or irritated skin

do not bandage or cover with any type of wrap except clothing

do not use with a heating pad or apply external heat

do not use 1 hour prior to bathing or within 30 minutes after bathing

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

If pregnant or breast feeding：

If pregnant or breast feeding, ask a health professional before use.

PURPOSE

Topical analgesic

QUESTION

None

STOP USE

Condition worsens,

Severe skin irritation occurs

Pain persist for more than 7 days

Symptoms clear up and occur again within a few days.

You experience pain, swelling or blistering, as rare but serious burns can occur

headache or redness occurs

When using this product：：

Use only as directed

do not get into eyes or on mucous membranes. If contact occurs, rinse thoroughly with water

do not apply to wounds, damaged or irritated skin

do not bandage or cover with any type of wrap except clothing

do not use with a heating pad or apply external heat

do not use 1 hour prior to bathing or within 30 minutes after bathing

Warnings

For external use only.

Other information

This product may cause allergic reaction on some individuals

Store in cool dry place away from direct sunlight

Store at 15-30°C (59-86°F)

Inactive ingredients

Acrylamide/Sodium Acryloyldimethyltaurate Copolymer, Dihydroxyaluminum aminoacetate, DMDM hydantoin, Edetic acid, Glycerin, Laurocapram, Polyacrylic acid, Sodium polyacrylate, Tartaric acid, Titanium dioxide, Water

STORE

Store in cool dry place away from direct sunlight

Store at 15-30°C (59-86°F)

Directions

Adults and children 12 years of age and older:apply to affected area; change patch 1 to 2 times daily

Children under 12 years of age: consult a doctor before use

How to Apply：

Clean and dry affected area

Cut open pouch and remove patch

Remove protective film and apply directly to area of pain

Apply to affected area not more than 3 times daily. Do not leave on skin for more than a total of 8 hours per day

Wash hands with soap after applying patch

Reseal pouch containing unused patches

Children under 2 years of age: do not use, consult a physician

Directions

Adults and children 12 years of age and older:apply to affected area; change patch 1 to 2 times daily

Children under 12 years of age: consult a doctor before use

How to Apply

Clean and dry affected area

Cut open pouch and remove patch

Remove protective film and apply directly to area of pain

Apply to affected area not more than 3 times daily. Do not leave on skin for more than a total of 8 hours per day

Wash hands with soap after applying patch

Reseal pouch containing unused patches

Children under 2 years of age: do not use, consult a physician

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

RAPID RELIEF 
pain relief patch patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83569-008
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	110 mg
CAPSICUM (UNII: 00UK7646FG) (CAPSICUM - UNII:00UK7646FG)	CAPSICUM	22 mg
LEVOMENTHOL (UNII: BZ1R15MTK7) (LEVOMENTHOL - UNII:BZ1R15MTK7)	LEVOMENTHOL	33 mg

Inactive Ingredients
Ingredient Name	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
ACRYLAMIDE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (120000 MPA.S AT 1%) (UNII: 5F4963KLHS)
TARTARIC ACID (UNII: W4888I119H)
EDETIC ACID (UNII: 9G34HU7RV0)
SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
GLYCERIN (UNII: PDC6A3C0OX)
DMDM HYDANTOIN (UNII: BYR0546TOW)
DIHYDROXYALUMINUM AMINOACETATE ANHYDROUS (UNII: 1K713C615K)
LAUROCAPRAM (UNII: 1F3X9DRV9X)
POLYACRYLIC ACID (800000 MW) (UNII: D0I6NSZ87U)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83569-008-02	5 in 1 BOX	07/31/2025
1	NDC: 83569-008-01	1 in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	07/31/2025

Labeler - RAPID AID VIET NAM COMPANY LIMITED (673067008)

Registrant - RAPID AID VIET NAM COMPANY LIMITED (673067008)

Establishment
Name	Address	ID/FEI	Business Operations
RAPID AID VIET NAM COMPANY LIMITED		673067008	manufacture(83569-008)