FDA Label for Numbr-x
View Indications, Usage & Precautions
Numbr-x Product Label
The following document was submitted to the FDA by the labeler of this product Prodigy Media 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.
Active Ingredient
Lidocaine HCL 4%
Purpose
External Analgesic
Uses
For the temporary relief of pain and itching associated with sunburns, minor cuts, insect bites, and skin irritations
Warnings
- For external use only.
- Avoid contact with eyes
- Condition worsens or symptoms persist for more than 7 days
- Symptoms clear up and occur again within a few days
- Do not use in large quantities, particularly over raw surfaces or blistered areas. Do not exceed the recommended daily dosage unless directed by a doctor.
- On wounds or damaged skin.
Stop use and ask a doctor if
Do not use
Keep Out Of Reach Of Children
If product is swallowed, get medical help or contact a Poison Control Center right away.
Direction
Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 2 years of age: do not use, consult a physician.
Other Information
Do not use if seal is broken.
Inactive Ingredients
Aqua (Deionized Water), Arnica Montana Flower Extract,C13-14 Isoparaffin, Chondroitin Sulfate, Dimethyl Sulfone (MSM), Emu Oil,
Ethoxydiglycol, Ethylhexylglycerin, Glucosamine Sulfate, Isopropyl Palmitate, Laureth-7, Phenoxyethanol, Polyacrylamide, Propylene Glycol, Stearic Acid,Tea Tree Oil, Triethanolamine.
Product Label
* Please review the disclaimer below.
