Dermoplast Anesthetic Pain and Itch

Product NDC

68754-680

11-digit product format

687540680

Labeler code

68754

Product ID

68754-680_9b0277b1-b584-b2db-e053-2995a90aa194

Type

HUMAN OTC DRUG

Nonproprietary name

BENZOCAINE, MENTHOL

Dosage form

SPRAY

Route

TOPICAL

Labeler

American Spraytech, LLC

Application

part348

Marketing category

OTC MONOGRAPH NOT FINAL

Marketing start

2014-01-01

Marketing end

0000-00-00

Substance

BENZOCAINE; MENTHOL, UNSPECIFIED FORM

Active strength

200 mg/g; mg/g

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record