FDA Label for Pain Relief Gel
View Indications, Usage & Precautions
Pain Relief Gel Product Label
The following document was submitted to the FDA by the labeler of this product Kanamed Inc.. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Otc - 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
- 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.