Numb520Spray
Numb520Spray is an FDA drug label for the active ingredient LIDOCAINE, PHENYLEPHRINE HCL manufactured by Ebanel Laboratories, Inc. administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260820.
- Generic name
- LIDOCAINE, PHENYLEPHRINE HCL
- Manufacturer
- Ebanel Laboratories, Inc.
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 72654-037
- Application
- M015
- Label effective
- 20260820
About this product
Numb520Spray is an FDA-registered drug product whose active ingredient is LIDOCAINE, PHENYLEPHRINE HCL. It is labelled by Ebanel Laboratories, Inc. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 72654-037, application M015, label effective 20260820. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.
What it is used for
Across FDA labelling, products containing LIDOCAINE, PHENYLEPHRINE HCL are most often described in connection with: temporary relief, anorectal disorders, discomfort associated, pain burning, soreness temporarily, shrinks hemorrhoidal, irritation hemorrhoids. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses ■ For the temporary relief of local and anorectal itching and discomfort associated with anorectal disorders and anorectal inflammation. ■ For the temporary relief of pain, burning and soreness. ■ Temporarily shrinks hemorrhoidal tissue. ■ Temporarily reduces the swelling associated with irritation in hemorrhoids and other anorectal disorders.
Dosage & Administration
Directions ■ Adults: When practical, cleanse the affected area with mild soap and warm water and rinse thoroughly. Gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product. Children under 12 years of age: consult a doctor. ■ Apply externally to the affected area up to 4 times daily.
Warnings
Warnings ■ 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. ■ Certain persons can develop allergic reactions to ingredients in this product. If the symptom being treated does not subside or if redness, irritation, swelling, pain, or other symptoms develop or increase, discontinue use and consult a doctor. ■ Do not use this product if you have heart disease, high blood pressure, thyroid disease, diabetes, or difficulty in urination due to enlargement of the prostate gland unless directed by a doctor. ■ Ask a doctor or pharmacist before use if you are presently taking a prescription drug for high blood pressure or depression.
Frequently asked questions
What is Numb520Spray used for?
Uses ■ For the temporary relief of local and anorectal itching and discomfort associated with anorectal disorders and anorectal inflammation. ■ For the temporary relief of pain, burning and soreness. ■ Temporarily shrinks hemorrhoidal tissue. ■ Temporarily reduces the swelling associated with irritation in hemorrhoids and other anorectal disorders.
Who makes Numb520Spray?
Ebanel Laboratories, Inc. is the labeler of record for Numb520Spray.
What form does Numb520Spray come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is Numb520Spray prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.
Has Numb520Spray been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.
Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.