zourunan PAIN RELIEF

Manufacturer
Guchutang Biotechnology (Longyan) Co., Ltd
Effective date
2025-10-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:40:48

Label at a glance#

Productzourunan PAIN RELIEF
Active ingredientCAMPHOR (NATURAL), CAPSAICIN, METHYL SALICYLATE
Label structure12 sections

Dosage and administration

Apply a thin layer of spray to the affected area as soon as possible after minor injury.Repeat 3 times a day or as needed. if heat or ice is applied, wait 5 minutes before applying spray.Children under 2 years of age: do not use, consult a physician or doctor.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Methyl salicylate 30%
Capsaicin 0.025%
Camphor 5%

Purpose

OTC - PURPOSE SECTION

Topical analgesic

Use

INDICATIONS & USAGE SECTION

Temporarily relieves muscle and stiffness due to:
■minor injuries
■overexertion
■falls reduces symptoms of bruising such as
■pain■swelling■discoloration

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

you are allergic to spray or to any of this product's inactive ingredients.

When Using

OTC - WHEN USING SECTION

Avoid contact with eyes, mucous mem branes, wounds, damaged or irritated skin. Use only directed dryness or irritation may occurdo not tightly wrap or bandage the treated area do not apply heat or ice to treated area immediately before or after use.

Stop Use

OTC - STOP USE SECTION

Condition persists for more than 3 days or worsens osymptoms clear up and occur again within a few days.

Ask Doctor

OTC - ASK DOCTOR SECTION

Condition persists for more than 3 days or worsens osymptoms clear up and occur again within a few days.

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

Apply a thin layer of spray to the affected area as soon as possible after minor injury.Repeat 3 times a day or as needed. if heat or ice is applied, wait 5 minutes before applying spray.Children under 2 years of age: do not use, consult a physician or doctor.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Ethanol, water, Caramel color

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2727391camphor 5 % / capsaicin 0.025 % / methyl salicylate 30 % Topical SprayPSN1
2727391camphor 50 MG/ML / capsaicin 0.25 MG/ML / methyl salicylate 300 MG/ML Topical SpraySCD1
2727391camphor 5 % / capsaicin 0.025 % / methyl salicylate 30 % Topical SpraySY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
473d070d-1c38-488e-b991-c4d1bf45aab8Product name120210201
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87083-006-01zourunan PAIN RELIEF100 mL in 1 BOTTLE, SPRAYSPRAY1001

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87083-00687083-006-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
zourunan PAIN RELIEFPAIN RELIEFGuchutang Biotechnology (Longyan) Co., Ltd41bc1c0c-63d5-0d41-e063-6394a90a341b2025-10-22WarningsExact identifier
ndc (package): 87083-006-01
ndc (product): 87083-006
ndc11 (package): 87083000601
spl id: 41bc1c0c-63d6-0d41-e063-6394a90a341b
spl set id: 41bc1c0c-63d5-0d41-e063-6394a90a341b

Reported adverse events (FAERS/openFDA)#

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