Iontocaine

{{Short description|Chemical compound}}

{{Drugbox

| verifiedrevid = 447388779

| type = combo

| component1 = Lidocaine

| class1 = Local anesthetic

| component2 = Epinephrine

| class2 = Vasoconstrictor

| tradename =

| pregnancy_AU =

| pregnancy_US =

| pregnancy_category =

| legal_AU =

| legal_CA =

| legal_UK =

| legal_US =

| legal_US_comment = Approved in 1995, discontinued in 2005

| routes_of_administration = Topical

| CAS_number_Ref = {{cascite|correct|??}}

| CAS_number = 54958-67-7

| ATCvet =

| ATC_prefix =

| ATC_suffix =

| PubChem =

| DrugBank_Ref = {{drugbankcite|correct|drugbank}}

| DrugBank =

}}

Iontocaine was an anesthetic medication, marketed under the two brand names Numby and Phoresor PM900 by IOMED inc. It is a local anesthetic with vasoconstrictor, administered via iontophoresis through the skin. It can numb up to 10 mm of skin in as little as 10 minutes. It is a 2% lidocaine, 0.01 mg/ml epinephrine solution. It was manufactured by IOMED, Inc.

Iontocaine was approved by the United States Food and Drug Administration on 21 December 1995.[https://www.accessdata.fda.gov/scripts/cder/daf/ United States Food and Drug Administration, Drug Approval Reports] It was discontinued by the manufacturer in 2005.United States Food and Drug Administration, August 2005: Additions and Deletions to the Drug Product List. [https://web.archive.org/web/20090601054914/http://www.fda.gov/Drugs/default.htm]