FDA Label for Quick Numb
View Indications, Usage & Precautions
Quick Numb Product Label
The following document was submitted to the FDA by the labeler of this product Clinical Resolution Laboratory, 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 5%
Purpose
Local Anesthetic
Uses:
For the temporary relief of local and anorectal discomfort associated with anorectal discomfort or inflammation.
Warnings
(For external use only)
Do Not Use This Product If
When Using This Product
- Do not exceed the recommended daily dosage unless directed by a doctor.
- Certain persons can develop allergic reactions to ingredients in this product.
- Do not put this product into the rectum by using fingers or any medical device or applicator.
Stop Use And Ask A Doctor If
The symptom being treated does not subside, or if redness, irritation, swelling, pain, or other symptoms develop or increase.
Keep Out Of Reach Of Children
In case of accidental ingestion, seek medical attention immediately.
Directions
- Adults: When practical, cleanse the affected area with mild soap and warm water and rise thoroughly. Gently dry by patting or blotting with toilet tissue or a soft cloth, before application of this product.
- Apply up to 6 times a day.
- Children under 12 years of age: consult a doctor.
Other Information
- Keep away from direct sunlight or heat.
- Store in room temperature (59-86°F / 15-30°C).
Inactive Ingredients
Allanloin, Aloe Barbadensis Leaf Juice, Benzyt Alcohol,Carbomer, Cholesterol, Dlmethyt lsosorbide, DisodiumEDTA, Hydrogenated Polydecene, Lecithin, NeopenlytGlycol Dicaprylale/Dicaprate. Propylene Glycol, Water,Sodium Polyacrytate, Tocopheryt Acetate, Trideceth-6,Triethanolamine
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