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Derma Numb (Lidocaine hydrochloride) Package Insert

Status:
Prescription (Rx) Facts
Strength:
40 mg/g
Other brand names:
Drug class:
Active ingredient:
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Source: FDA drug labeling via NLM DailyMed · About this document

Prescribing information (package insert) - Derma Numb

Active Ingredients

Lidocaine HCI

Purpose

Topical Anesthetic

Uses

Temporarily relieves pain from tattoo procedures.

Directions

First test product to sensitivity to skin.

Once skin is broken or outline is done, apply derma numb generously to tattooed area.

Wait two minutes for anesthetic to take affect, re-apply derma numb to tattoo area as needed through out the tattoo process for comfort. Discontinue use if sensitivity occurs. Do not use on face.

Warnings

External Use Only

Avoid contact with the eyes

Do Not Use

If you have any known allergy or sensitivity to any of these ingredients in this product. Discontinue use and seek medical attention.

Stop Use and ask a doctor if

  • skin becomes irritated • condition worsens or symptoms last more than7 days • symptoms clear up and reoccur with a few days

Inactive ingredients

Water, Propylene Glycol, Achillea Millefolium (Yarrow) Extract, Yucca Glauca Root Extract, Citric Acid, Sodium Metabisulfate, Caprylyl Glycol, Disodium EDTA, Methylisothiazolinone.

Other Information

This product was manufactured for Atlas Tat, Inc.

Any questions call 954-492-9898 or check out the web @ dermnumb.com

About this document

Source: FDA drug labeling via NLM DailyMed · Application number: OTC MONOGRAPH FINAL 348 · View the label on DailyMed

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The information on this site does not replace the advice of a doctor or pharmacist.

Drug information for Derma Numb

Rx or OTC
Prescription (Rx)?
  • This drug is available only with a prescription from a licensed healthcare provider.
  • Rx
Drug class Amide Local Anesthetic, Antiarrhythmic
Active ingredient Lidocaine hydrochloride 40 mg/g
Dosage form Spray
Route Topical
Marketing status not in the current FDA NDC Directory
Company (applicant) Atlas Tat Inc.
FDA approval OTC MONOGRAPH FINAL 348OTC monograph
Manufacturers 1 labelers list this drug on DailyMed
Packages (NDC)
Package
40 mg/g – 28.35 g in 1 bottle, spray NDC 53200-001-01

Source: FDA drug labeling via NLM DailyMed, data as of November 3, 2026. FDA data (DailyMed, Orange Book, Drug Shortages, enforcement reports). Not a substitute for the advice of a doctor or pharmacist.