Home > National Drug Code (NDC) > I-MAX LIGHTENING 5

I-MAX LIGHTENING 5 - 42952-201-12 - (HYDROQUINONE)

Alphabetical Index


Drug Information of I-MAX LIGHTENING 5

Product NDC: 42952-201
Proprietary Name: I-MAX LIGHTENING 5
Non Proprietary Name: HYDROQUINONE
Active Ingredient(s): 2    g/100g & nbsp;   HYDROQUINONE
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of I-MAX LIGHTENING 5

Product NDC: 42952-201
Labeler Name: MAXLIFE USA, INC.
Product Type: HUMAN OTC DRUG
FDA Application Number: part358A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120918

Package Information of I-MAX LIGHTENING 5

Package NDC: 42952-201-12
Package Description: 59 g in 1 TUBE (42952-201-12)

NDC Information of I-MAX LIGHTENING 5

NDC Code 42952-201-12
Proprietary Name I-MAX LIGHTENING 5
Package Description 59 g in 1 TUBE (42952-201-12)
Product NDC 42952-201
Product Type Name HUMAN OTC DRUG
Non Proprietary Name HYDROQUINONE
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20120918
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name MAXLIFE USA, INC.
Substance Name HYDROQUINONE
Strength Number 2
Strength Unit g/100g
Pharmaceutical Classes

Complete Information of I-MAX LIGHTENING 5


General Information