NUMSTAT Antiseptic and Pain Relieving Prep Pad
NUMSTAT Antiseptic and Pain Relieving Prep Pad is an FDA drug label for the active ingredient ALCOHOL, MENTHOL, AND BENZOCAINE PREP PAD manufactured by Spectra Medical Devices, LLC 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 20231220.
- Generic name
- ALCOHOL, MENTHOL, AND BENZOCAINE PREP PAD
- Manufacturer
- Spectra Medical Devices, LLC
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 65282-1815
- Application
- M003
- Label effective
- 20231220
About this product
NUMSTAT Antiseptic and Pain Relieving Prep Pad is an FDA-registered drug product whose active ingredient is ALCOHOL, MENTHOL, AND BENZOCAINE PREP PAD. It is labelled by Spectra Medical Devices, LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 65282-1815, application M003, label effective 20231220. 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 ALCOHOL, MENTHOL, AND BENZOCAINE PREP PAD are most often described in connection with: temporary relief, pain associated, needle sticks, minor burns, cuts scrapes, skin irritations, insect bites, risk infection. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses Uses • For the temporary relief of pain associated with needle sticks, minor burns, sunburn, minor cuts, scrapes, minor skin irritations, and insect bites • Reduces the risk of infection • Kills germs
Dosage & Administration
Directions Directions for Use Adults and children 2 years of age and older. • Apply to affected area. Do not apply more than 4 times daily. • Apply pad solution to the skin and gently rub in and let dry. • Test for effect by touching area before performing procedure May need to reapply on certain skin types. For children under 2 years of age, consult a doctor.
Warnings
Warnings Warnings Flammable . Keep away from heat or open flame. When using this product • Use glove with application hand or always wash application hand immediately after application For external use only
Recall and safety notices
1 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.
| Recall | Product | Firm | Class | Status | Reported |
|---|---|---|---|---|---|
| D-0554-2026 | Lidocaine HCl Injection USP, 25x5 mL, Single-Dose Ampules, Rx Only, Distributed by: Spectra Medical Devices, LLC, Wilmington, Made in S. Korea, NDC 65282-1605-1. | Spectra Medical Devices, Llc | Class II | Ongoing | 20260610 |
Frequently asked questions
What is NUMSTAT Antiseptic and Pain Relieving Prep Pad used for?
Uses Uses • For the temporary relief of pain associated with needle sticks, minor burns, sunburn, minor cuts, scrapes, minor skin irritations, and insect bites • Reduces the risk of infection • Kills germs
Who makes NUMSTAT Antiseptic and Pain Relieving Prep Pad?
Spectra Medical Devices, LLC is the labeler of record for NUMSTAT Antiseptic and Pain Relieving Prep Pad.
What form does NUMSTAT Antiseptic and Pain Relieving Prep Pad 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 NUMSTAT Antiseptic and Pain Relieving Prep Pad 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 NUMSTAT Antiseptic and Pain Relieving Prep Pad been recalled?
1 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.
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.