Pain Relief Gel

Manufacturer: Kanamed Inc.
Effective date: 2019-10-24
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:01:19

Label at a glance#

ProductPain Relief Gel

Active ingredientMENTHOL, CAMPHOR (NATURAL)

Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Menthol 5% Topical Analgesic

Camphor 5% Topical Analgesic

INDICATIONS & USAGE SECTION

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

arthritis
simple backache
muscle strains
bruises
sprains

INACTIVE INGREDIENT SECTION

Hemp seed oil
Aloe vera Juice
Peppermint Oil
Ethylenediaminetetraacetic Acid
Glycerine
Carbopol U10
Caustic Soda/Sodium hydroxide
Propylene Glycol
Sodium Benzonate
DM Water

DOSAGE & ADMINISTRATION SECTION

Use only as directed
Adults and children 12 years of age and older apply to affected area not more than 3 to 4 times daily
Children under the age of 12 years of age consult a doctor

WARNINGS SECTION

For external use only
Only use as directed
Do not allow contact with eyes
Do not bandage tightly

STOP use and ask a doctor if:

symptoms last more than 7 days or clear up and occur again within a few days
Excessive skin irritation occurs
If you have redness over the affected area

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OTC - PURPOSE SECTION

Topical Analgesic

OTHER SAFETY INFORMATION

Store at room temperature

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PAIN RELIEF copy

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
73239-1904-1	2021-01-29	C162847	48780-1	ba0f9c33-4860-a910-e053-dadaa90a0b85	Pain Relief Gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73239-1904-1	Pain Relief Gel	100 mL in 1 TUBE	GEL	100		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73239-1904	PAIN RELIEF GEL (CAMPHOR, AND MENTHOL GEL) GEL [KANAMED INC.]	1	Legacy NDC, 1 package rows	20191025_95ae7b57-3e85-db85-e053-2995a90a741f.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

Pain Relief Gel
Camphor, and Menthol gel
ALOE VERA WHOLE
MENTHOL
HEMP
WATER
CAMPHOR (NATURAL)

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73239-1904	73239-1904-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALOE VERA WHOLE	KIZ4X2EHYX	IACT
MENTHOL	L7T10EIP3A	ACTIB
HEMP	TD1MUT01Q7	IACT
WATER	059QF0KO0R	IACT
CAMPHOR (NATURAL)	N20HL7Q941	ACTIB

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
95ae7b69-107c-e959-e053-2a95a90a35fe			95ae7b57-3e85-db85-e053-2995a90a741f	2019-10-24	Warnings	Exact identifier spl id: 95ae7b69-107c-e959-e053-2a95a90a35fe spl set id: 95ae7b57-3e85-db85-e053-2995a90a741f

Reported adverse events (FAERS/openFDA)#

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