PAIN RELIEF GEL- camphor, and menthol gel gel

Pain Relief Gel by

Drug Labeling and Warnings

Pain Relief Gel by is a Otc medication manufactured, distributed, or labeled by Kanamed Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Menthol 5% Topical Analgesic

Camphor 5% Topical Analgesic

INDICATIONS & USAGE

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

• arthritis
• simple backache
• muscle strains
• bruises
• sprains

INACTIVE INGREDIENT

• 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

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

• 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

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

PURPOSE

Topical Analgesic

OTHER SAFETY INFORMATION

Store at room temperature

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PAIN RELIEF GEL 
camphor, and menthol gel gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73239-1904
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	5 mg  in 100 mL
CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941)	CAMPHOR (NATURAL)	5 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA WHOLE (UNII: KIZ4X2EHYX)
HEMP (UNII: TD1MUT01Q7)
WATER (UNII: 059QF0KO0R)	1 mg  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73239-1904-1	100 mL in 1 TUBE; Type 0: Not a Combination Product	10/16/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	10/16/2019

Labeler - Kanamed Inc. (117131580)

Registrant - Kanamed Inc. (117131580)