FDA Label for Numpot Topical Anesthetic
View Indications, Usage & Precautions
Numpot Topical Anesthetic Product Label
The following document was submitted to the FDA by the labeler of this product Unit Dose, Ltd.. 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 5%
Petrolatum 71%
Purpose
Anesthetic
Skin Protectant
Uses:
Temporarily relieves local discomfort, pain and Swelling, or burning associated with anorectal disorders.
Warning:
External use only. Keep out of eyes. Allergic reactions can occur.
Stop Use & Ask A Doctor:
If condition worsens or does not improve within 7 days
- If redness, irritation, pain, swelling or other symptoms develop or increase
- If bleeding occurs.
Keep Out Of Reach Of Children:
If swallowed get medical help or contact a Poison Control Center ASAP.
Directions:
Apply sparingly to affected area as often as needed up to 6 times daily.
​STORE IN COOL DARK AREA.
Inactive Ingredients:
Mineral Oil, Lanolin Alcohol, Polysorbate 60, Paraffin, Sorbitan Oleate, Tocopheryl Acetate (Vit. E Acetate), Aloe Barbadensis (Organic Aloe Vera) leaf juice, Cholecalciferol (Vit. D3), Phytonadione (Vit. K1)
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