Nekvnro Horse Paste. Hydrogel Pain Relief Patch

Manufacturer
Guoyu Trading Co., Ltd.
Effective date
2024-11-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:34:11

Label at a glance#

ProductNekvnro Horse Paste. Hydrogel Pain Relief Patch
Active ingredientCAPSAICIN, CAMPHORIC ACID, (-)-
Label structure13 sections

Dosage and administration

Adults and children 12 years of age and over ■ clean and dry affected area ■ remove film from patch and apply to the skin ■ apply 1 patch at a time to affected area, not more than 3 to 4 times daily ■ remove patch from the skin after at most 8 hours of application Children under 12 years of age: consult a doctor

Storage and handling

■ avoid storing product in direct sunlight ■ protect product from excessive moisture ■ Store in a cool, dry place within 2-25°C(36-77°F)

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Capsaicin 0.025%
Camphor 1%

Purpose

OTC - PURPOSE SECTION

Relieve joint pain
Reduce swelling and relieve pain

Use

INDICATIONS & USAGE SECTION

temporarily relieves minor aches and pains of muscles and joints associated with:

■simple backache

■arthritis

■strains

■ bruises

■ sprains

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

■ on wounds or damaged skin
■ with a heating pad
■ if you have ever had an allergic reaction to this product or any of its ingredients

When Using

OTC - WHEN USING SECTION

■ use only as directed
■ avoid contact with the eyes, mucous membranes or rashes
■ do not bandage tightly

Stop Use

OTC - STOP USE SECTION

■ localized skin reactions occur, such as rash, itching, redness, irritation, pain swelling and blistering
■ conditions worsen
■ symptoms persist for more than 7 days
■ symptoms clear up and occur again within a few days
If pregnant or breast-feeding should not use this product.

Ask Doctor

OTC - ASK DOCTOR SECTION

■ localized skin reactions occur, such as rash, itching, redness, irritation, pain swelling and blistering
■ conditions worsen
■ symptoms persist for more than 7 days
■ symptoms clear up and occur again within a few days
If pregnant or breast-feeding should not use this product.

Keep Oot 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 over
■ clean and dry affected area
■ remove film from patch and apply to the skin
■ apply 1 patch at a time to affected area, not more than 3 to 4 times daily
■ remove patch from the skin after at most 8 hours of application Children under 12 years of age: consult a doctor

Other information

STORAGE AND HANDLING SECTION

■ avoid storing product in direct sunlight
■ protect product from excessive moisture
■ Store in a cool, dry place within 2-25°C(36-77°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified water,glycerin,Ethylhexylglycerin,Phenoxyethanol,Disodium oxalate,Sodium polyacrylate,Propylene glycol,peppermint

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1122334455

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
473d070d-1c38-488e-b991-c4d1bf45aab8Product name120210201

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84844-011-01Nekvnro Horse Paste. Hydrogel Pain Relief Patch10 in 1 BOXPATCH101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84844-011NEKVNRO HORSE PASTE. HYDROGEL PAIN RELIEF PATCH (HORSE PASTE HYDROGEL PAIN RELIEF PATCH) PATCH [GUOYU TRADING CO., LTD.]11 package rows20241106_2626baeb-8c6c-5991-e063-6294a90ab550.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84844-01184844-011-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
2626baeb-8c6d-5991-e063-6294a90ab5502626baeb-8c6c-5991-e063-6294a90ab5502024-11-05WarningsExact identifier
spl id: 2626baeb-8c6d-5991-e063-6294a90ab550
spl set id: 2626baeb-8c6c-5991-e063-6294a90ab550

Reported adverse events (FAERS/openFDA)#

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