LINGRUI Bone Strength Musk Pain Relief Cream

Manufacturer
Dengfeng City Jucai Trading Co., LTD
Effective date
2023-11-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:02:38

Label at a glance#

ProductLINGRUI Bone Strength Musk Pain Relief Cream
Active ingredientMENTHOL
Label structure12 sections

Dosage and administration

Apply the adhesive side of the patch to the affected area. Use one patch for up to 8 hours

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 4%

Purpose

OTC - PURPOSE SECTION

Dispelling wind and dampness, promoting blood circulation and relieving pain. Used for rheumatic joints, muscle pain, and sprains.

Use

INDICATIONS & USAGE SECTION

for external use

Warnings

WARNINGS SECTION

This product may cause itching, tingling, rash (such as erythema, papules, blisters), local edema, skin ulceration, and in rare cases, systemic discomfort.

Do not use

OTC - DO NOT USE SECTION

1. Prohibited for pregnant women.

2. Prohibited for infants and young children.

3. Prohibited for skin ulcers, skin lesions, or infected areas.

4. It is prohibited for those who are allergic to this product and its ingredients (including excipients).

5. It is prohibited for those who are allergic to rubber paste.

When Using

OTC - WHEN USING SECTION

Lingrui Bone Strengthening Musk Pain Relieving Cream needs to be replaced every 24 hours

Stop Use

OTC - STOP USE SECTION

Itching, tingling, rash (such as erythema, papules, blisters), local edema caused by medication, skin ulceration, etc

Ask Doctor

OTC - ASK DOCTOR SECTION

Diabetes patients ask the doctor

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Please keep this product out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply the adhesive side of the patch to the affected area. Use one patch for up to 8 hours

Inactive ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredients.Raw Cao Wu,Raw Kawashima Frankincense,myrrh,
raw strychnine, cloves, cinnamon, thorns,windbreaks, stork's-bill, incense,
snowdrops, bones
Cortex Eucommiae, Angelica dahurica, Silybum marianum, Dried ginger, Methyl
salicylate
lce chips, camphor, rue infusion, belladonna flowManufactured for
extract. Excipients are: rubber, rosin,
zinc oxide, sheep's .Hair fat, petroleum
jelly, liquid paraffin,Dimethyl Sulfoxide,

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1122

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
853276menthol 4 % Medicated PatchPSN1
853276menthol 0.04 MG/MG Medicated PatchSCD1
853276menthol 4 % Medicated PatchSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83806-001-012025-01-30C16284748780-12cef2736-9cfc-d83d-e063-dadaa90ab31f0a8cd5a7-77d2-84e3-e063-6394a90a7eda

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83806-001-01LINGRUI Bone Strength Musk Pain Relief Cream1 in 1 BAGPATCH11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83806-001LINGRUI BONE STRENGTH MUSK PAIN RELIEF CREAM (BONE STRENGTH MUSK PAIN RELIEF CREAM) PATCH [DENGFENG CITY JUCAI TRADING CO., LTD]11 package rows20231123_0a8cd5a7-77d2-84e3-e063-6394a90a7eda.zip

Products#

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

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83806-00183806-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 24 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
0a8cd5a7-77d3-84e3-e063-6394a90a7eda0a8cd5a7-77d2-84e3-e063-6394a90a7eda2023-11-19WarningsExact identifier
spl id: 0a8cd5a7-77d3-84e3-e063-6394a90a7eda
spl set id: 0a8cd5a7-77d2-84e3-e063-6394a90a7eda

Reported adverse events (FAERS/openFDA)#

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