NDC Code(s) : 50804-024-08
Packager : Good Sense

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Patch Menthol PATCH
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:50804-024
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MENTHOL(UNII: L7T10EIP3A)
(MENTHOL - UNII:L7T10EIP3A) 		MENTHOL775 mg
Inactive Ingredients
Ingredient Name Strength
ALCOHOL(UNII: 3K9958V90M)
ALUMINUM HYDROXIDE(UNII: 5QB0T2IUN0)
BORNEOL(UNII: M89NIB437X)
CAMPHOR (NATURAL)(UNII: N20HL7Q941)
EDETATE DISODIUM(UNII: 7FLD91C86K)
GLYCERIN(UNII: PDC6A3C0OX)
METHYLPARABEN(UNII: A2I8C7HI9T)
PROPYLPARABEN(UNII: Z8IX2SC1OH)
POVIDONE(UNII: FZ989GH94E)
SODIUM POLYACRYLATE (8000 MW)(UNII: 285CYO341L)
TARTARIC ACID(UNII: W4888I119H)
TITANIUM DIOXIDE(UNII: 15FIX9V2JP)
WATER(UNII: 059QF0KO0R)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:50804-024-085 in 1 BOX 02/11/2016
11 in 1 POUCH Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part348 11/02/2016

PRINCIPAL DISPLAY PANEL

image description