Otc - Active Ingredient
Menthol 5% Topical Analgesic
Camphor 5% Topical Analgesic
Pain Relief Gel
FDA Label NDC 73239-1904
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Kanamed Inc. for the product Pain Relief Gel (NDC 73239-1904). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, indications & usage, inactive ingredient, dosage & administration, warnings, otc - keep out of reach of children, otc - purpose, other safety information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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
- 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
STOP use and ask a doctor if:
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Otc - Purpose
Topical Analgesic
Other Safety Information
Store at room temperature
* Please review the disclaimer below.
