Enzoclear Foam

Product NDC: 73159-001
11-digit product format: 731590001
Labeler code: 73159
Product ID: 73159-001_2ae18d12-1bb8-4e75-bb45-dbf3db10c9be
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Benzoyl Peroxide
Dosage form: AEROSOL, FOAM
Route: TOPICAL
Labeler: Lacer Pharma, LLC
Marketing category: UNAPPROVED DRUG OTHER
Marketing start: 2019-07-25
Marketing end: 0000-00-00
Substance: BENZOYL PEROXIDE
Active strength: 10 g/g
NDC exclude flag: No
Listing certified through: 2023-12-31
Current FDA listing: Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
73159-001-01	GM - Gram	73159-001	1261ea96-ee77-433f-90fe-370c9e08e1f5	1	2019-12-10

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
73159-001-01	73159000101	100 g in 1 CAN (73159-001-01)	100 g	2019-07-25	0000-00-00	No	No	Current