Lanolin - 67777-232-04 - (Lanolin)

Alphabetical Index


Drug Information of Lanolin

Product NDC: 67777-232
Proprietary Name: Lanolin
Non Proprietary Name: Lanolin
Active Ingredient(s): 50    g/100g & nbsp;   Lanolin
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Lanolin

Product NDC: 67777-232
Labeler Name: Dynarex Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part347
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100512

Package Information of Lanolin

Package NDC: 67777-232-04
Package Description: 24 TUBE in 1 CASE (67777-232-04) > 113 g in 1 TUBE

NDC Information of Lanolin

NDC Code 67777-232-04
Proprietary Name Lanolin
Package Description 24 TUBE in 1 CASE (67777-232-04) > 113 g in 1 TUBE
Product NDC 67777-232
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Lanolin
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20100512
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Dynarex Corporation
Substance Name LANOLIN
Strength Number 50
Strength Unit g/100g
Pharmaceutical Classes

Complete Information of Lanolin


General Information