MEDICATED NO MESS APPLICATOR

Product NDC

52000-029

11-digit product format

520000029

Labeler code

52000

Product ID

52000-029_57fcd577-9455-4cee-e053-2991aa0a266b

Type

HUMAN OTC DRUG

Nonproprietary name

menthol

Dosage form

LIQUID

Route

TOPICAL

Labeler

Universal Distribution Center LLC

Application

part348

Marketing category

OTC MONOGRAPH NOT FINAL

Marketing start

2017-08-30

Marketing end

0000-00-00

Substance

MENTHOL

Active strength

0 g/mL

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record