Active Ingredients
Lidocaine HCL (5%)
Uber Numb Cream
FDA Label NDC 71131-051
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Uberscientific, Llc for the product Uber Numb (NDC 71131-051). 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 active ingredients, purpose, uses, warnings:, keep out of reach of children., directions:, inactive ingredients:, distributed by:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
External Analgesic
Uses
For the Temporary relief of pain and discomfort associated with anorectal disorders
Warnings:
For external ues only. If condition worsens or does not improve within 7 days, consult a doctor. Do not exceed the recommended daily dosage unless directed by a doctor. In case of bleeding, consult a doctor promptly. Do not put this product into the rectum by using fingers or any mechanical device or applicator.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact the Poison Control Center immediately
Directions:
Adults and children 12 years and older: For optimum results cleanse the affected area with mild soap and warm water and rinse thoroughly, Gently dry by patting or blotting with toilet tissue or a clean, soft cloth before application of this product.
Apply externally up to 6 times per day.
Children under 12: Consult a Doctor
Inactive Ingredients:
Allantoin Gel, Deionized Water, Benzyl Alcohol, Carbomer, Propylene Glycol, Sodium Polyacrylate, Tocopheryl Acetate (Vitamin E), Triethanolamine
Distributed By:
UberScientific LLC
838 E High St.
Ste 271
Lexington, KY 40502
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