Home > National Drug Code (NDC) > EB301AP PAIN RELIEF

EB301AP PAIN RELIEF - 53304-0301-3 - (MENTHOL)

Alphabetical Index


Drug Information of EB301AP PAIN RELIEF

Product NDC: 53304-0301
Proprietary Name: EB301AP PAIN RELIEF
Non Proprietary Name: MENTHOL
Active Ingredient(s): 1000    mg/100mL & nbsp;   MENTHOL
Administration Route(s): TOPICAL
Dosage Form(s): SPRAY
Coding System: National Drug Codes(NDC)

Labeler Information of EB301AP PAIN RELIEF

Product NDC: 53304-0301
Labeler Name: EMINENCE BIOTECH CORPORATION LIMITED
Product Type: HUMAN OTC DRUG
FDA Application Number: part348
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20130301

Package Information of EB301AP PAIN RELIEF

Package NDC: 53304-0301-3
Package Description: 1 BOTTLE, SPRAY in 1 BOX (53304-0301-3) > 15 mL in 1 BOTTLE, SPRAY

NDC Information of EB301AP PAIN RELIEF

NDC Code 53304-0301-3
Proprietary Name EB301AP PAIN RELIEF
Package Description 1 BOTTLE, SPRAY in 1 BOX (53304-0301-3) > 15 mL in 1 BOTTLE, SPRAY
Product NDC 53304-0301
Product Type Name HUMAN OTC DRUG
Non Proprietary Name MENTHOL
Dosage Form Name SPRAY
Route Name TOPICAL
Start Marketing Date 20130301
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name EMINENCE BIOTECH CORPORATION LIMITED
Substance Name MENTHOL
Strength Number 1000
Strength Unit mg/100mL
Pharmaceutical Classes

Complete Information of EB301AP PAIN RELIEF


General Information