Vaseline - 64942-1190-1 - (OCTISALATE, AVOBENZONE, ENSULIZOLE)

Alphabetical Index


Drug Information of Vaseline

Product NDC: 64942-1190
Proprietary Name: Vaseline
Non Proprietary Name: OCTISALATE, AVOBENZONE, ENSULIZOLE
Active Ingredient(s): 20; 15; 50; 13    mg/mL; mg/mL; mg/mL; mg/mL & nbsp;   OCTISALATE, AVOBENZONE, ENSULIZOLE
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Vaseline

Product NDC: 64942-1190
Labeler Name: CONOPCO Inc. d/b/a Unilever
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120801

Package Information of Vaseline

Package NDC: 64942-1190-1
Package Description: 600 mL in 1 BOTTLE (64942-1190-1)

NDC Information of Vaseline

NDC Code 64942-1190-1
Proprietary Name Vaseline
Package Description 600 mL in 1 BOTTLE (64942-1190-1)
Product NDC 64942-1190
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTISALATE, AVOBENZONE, ENSULIZOLE
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20120801
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name CONOPCO Inc. d/b/a Unilever
Substance Name AVOBENZONE; ENSULIZOLE; OCTISALATE; OCTOCRYLENE
Strength Number 20; 15; 50; 13
Strength Unit mg/mL; mg/mL; mg/mL; mg/mL
Pharmaceutical Classes

Complete Information of Vaseline


General Information