LUBRIDERM - 58232-0748-8 - (Avobenzone, Homosalate, Octisalate, Oxybenzone and Octocrylene)

Alphabetical Index


Drug Information of LUBRIDERM

Product NDC: 58232-0748
Proprietary Name: LUBRIDERM
Non Proprietary Name: Avobenzone, Homosalate, Octisalate, Oxybenzone and Octocrylene
Active Ingredient(s): 30; 60; 50; 35.5; 50    mg/g; mg/g; mg/g; mg/g; mg/g & nbsp;   Avobenzone, Homosalate, Octisalate, Oxybenzone and Octocrylene
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of LUBRIDERM

Product NDC: 58232-0748
Labeler Name: Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20100330

Package Information of LUBRIDERM

Package NDC: 58232-0748-8
Package Description: 227 g in 1 TUBE (58232-0748-8)

NDC Information of LUBRIDERM

NDC Code 58232-0748-8
Proprietary Name LUBRIDERM
Package Description 227 g in 1 TUBE (58232-0748-8)
Product NDC 58232-0748
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Avobenzone, Homosalate, Octisalate, Oxybenzone and Octocrylene
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20100330
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.
Substance Name AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Strength Number 30; 60; 50; 35.5; 50
Strength Unit mg/g; mg/g; mg/g; mg/g; mg/g
Pharmaceutical Classes

Complete Information of LUBRIDERM


General Information