Numpot Topical Anesthetic Ointment
FDA Label NDC 67194-018
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Unit Dose, Ltd. for the product Numpot Topical Anesthetic (NDC 67194-018). 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 drug facts, active ingredients, purpose, uses:, warning:, stop use & ask a doctor:, keep out of reach of children:, directions:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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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