Label: DERMA NUMB- lidocaine hci spray
- NDC Code(s): 53200-001-01
- Packager: Atlas Tat Inc.
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Updated October 3, 2012
If you are a consumer or patient please visit this version.
- Active Ingredients
Temporarily relieves pain from tattoo procedures.Close
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.Close
External Use Only
Avoid contact with the eyesClose
- 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.Close
- 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 daysClose
- Inactive ingredients
Water, Propylene Glycol, Achillea Millefolium (Yarrow) Extract, Yucca Glauca Root Extract, Citric Acid, Sodium Metabisulfate, Caprylyl Glycol, Disodium EDTA, Methylisothiazolinone.Close
- Other Information
This product was manufactured for Atlas Tat, Inc.
Any questions call 954-492-9898 or check out the web @ dermnumb.comClose
- INGREDIENTS AND APPEARANCE
lidocaine hci spray
Product Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:53200-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE 40 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM METABISULFITE (UNII: 4VON5FNS3C) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) EDETATE DISODIUM (UNII: 7FLD91C86K) ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK) YUCCA GLAUCA ROOT (UNII: 1A15YBH7N1) DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:53200-001-01 28.35 g in 1 BOTTLE, SPRAY Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part348 07/15/2012 Labeler - Atlas Tat Inc. (061275633)