FDA Label for Sunmed Motion
View Indications, Usage & Precautions
Sunmed Motion Product Label
The following document was submitted to the FDA by the labeler of this product Sunflora 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.
Drug Facts
Active Ingredients
Lidocaine 4%
Purpose
Topical Analgesic
Uses
Temporarily relieves minor pain associated with:
• arthritis • sprains • simple backache • muscle strains • cramps • bruises
Warnings
For external use only
When using this product
• use only as directed • do not bandage tightly • avoid contact with eyes • do not apply to wounds or damaged skin • do not use in large quantities, particularly over raw surfaces or blistered areas.
Stop use and ask a doctor if
• condition worsens • symptoms persist for more than 7 days • symptoms clear up and occur again within a few days
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
• Adults and children 2 years of age and older: Apply to the affected area not more than 3 to 4 times daily.
• Children under 2 years of age: Consult a doctor.
Inactive Ingredients
Allantoin, Caprylic/Capric Triglyceride, Capsicum Annuum Fruit Powder, Calcium Disodium EDTA, Cannabis Sativa (Aerial) Extract Oil, Dimethicone, dl-alpha Tocopheryl Acetate, Ethyl Alcohol, Ethylhexylglycerin, Ethylhexyl Stearate, Fragrance, Glycerin, Phenoxyethanol, Polysorbate 80, Propanediol, Propylene Glycol, Purified Water, Simethicone, Sodium Polyacrylate, Trideceth-6, Vitis Vinifera (Grape) Seed Oil, Xanthan Gum.
Packaging
* Please review the disclaimer below.