Medicated Balm Arthritis Pain Relieving Cream

Manufacturer: International Nature Nutraceuticals Inc. | Luoyang MuChun pharmaceutical Co., LTD
Effective date: 2017-09-26
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:52:36

Label at a glance#

ProductMedicated Balm Arthritis Pain Relieving Cream

Active ingredientCAMPHOR (NATURAL), MENTHOL

Label structure12 sections

Indications and uses

The temporary relief of minor aches and pains of muscles and joints due to: Simple backache Sprains Bruises Arthritis

Dosage and administration

Adults and children 2 years of age and older: Apply to affected area 3-4 times daily Children under 2 years of age: Do not use, consult a doctor

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Camphor 9%

Menthol 16%

Uses

OTC - PURPOSE SECTION

The temporary relief of minor aches and pains of muscles and joints due to:

Simple backache

Sprains

Bruises

Arthritis

Warnings

WARNINGS SECTION

For External use only

Do not use:

OTC - DO NOT USE SECTION

On wound or damaged skin

Otherwise than as directed

Stop using and consult with doctor if:

OTC - ASK DOCTOR SECTION

Condition worsens

symptoms persist for more than 7 days or clear up and occur again within a few days

allergic to salicylates or aspirin

Other Information

INDICATIONS & USAGE SECTION

Keep bottle tightly closed, store in a cool and dry place

Do not use if seal is broken

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 2 years of age and older: Apply to affected area 3-4 times daily

Children under 2 years of age: Do not use, consult a doctor

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, contact a doctor or poision control center immediately

Inactive Ingreidents

INACTIVE INGREDIENT SECTION

Eucalyptus oil

Petrolatum

Cinnamon bark oil

Paraffin

Ceresin

Peppermint oil

Pregnant or lactating women

OTC - PREGNANCY OR BREAST FEEDING SECTION

Consult a doctor before using

When using this product

OTC - WHEN USING SECTION

Avoid contact with the eyes, mouth, or mucous membranes

Do not bandage tightly

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
51367-032-75	2025-01-30	C162847	48780-1	2cef2736-5c83-d83d-e063-dadaa90ab31f	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
51367-032-75	Medicated Balm Arthritis Pain Relieving Cream	1 in 1 PACKAGE	CREAM	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51367-032	MEDICATED BALM ARTHRITIS PAIN RELIEVING CREAM (CAMPHOR, MENTHOL) CREAM [INTERNATIONAL NATURE NUTRACEUTICALS INC.]	1	Legacy NDC, 1 package rows	20171002_a3624554-57b5-4942-9a27-d95920615109.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

Medicated Balm Arthritis Pain Relieving Cream
Camphor, Menthol
CAMPHOR (NATURAL)
MENTHOL
EUCALYPTUS OIL
PETROLATUM
CINNAMON BARK OIL
PARAFFIN
CERESIN
PEPPERMINT OIL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
51367-032	51367-032-75

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CAMPHOR (NATURAL)	N20HL7Q941	ACTIB
MENTHOL	L7T10EIP3A	ACTIB
EUCALYPTUS OIL	2R04ONI662	IACT
PETROLATUM	4T6H12BN9U	IACT
CINNAMON BARK OIL	XE54U569EC	IACT
PARAFFIN	I9O0E3H2ZE	IACT
CERESIN	Q1LS2UJO3A	IACT
PEPPERMINT OIL	AV092KU4JH	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
d99da891-dba1-4707-98a6-9ff855655e8f			a3624554-57b5-4942-9a27-d95920615109	2017-09-26	Warnings	Exact identifier spl id: d99da891-dba1-4707-98a6-9ff855655e8f spl set id: a3624554-57b5-4942-9a27-d95920615109

Reported adverse events (FAERS/openFDA)#

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