Protocoxil

Product NDC: 71416-001
11-digit product format: 714160001
Labeler code: 71416
Product ID: 71416-001_b517b1db-6ee9-116a-e053-2995a90a71db
Type: HUMAN OTC DRUG
Nonproprietary name: BENZYL ALCOHOL
Dosage form: GEL
Route: TOPICAL
Labeler: Bio
Application: part348
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2017-05-09
Marketing end: 0000-00-00
Substance: BENZYL ALCOHOL
Active strength: 100 mg/g
NDC exclude flag: No
Listing certified through: 2021-12-31
Current FDA listing: Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1	Product name	1	20230829
3c386306-c48a-413e-bb69-70cb268496f3	Product name	1	20210727
9869efd7-d6dd-0665-5b67-53adbe6ef15e	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
71416-001-00	2022-01-28	C162847	48780-1	d6a99b39-9991-a426-e053-dadaa90af4c2	Protocoxil
71416-001-01	2022-01-28	C162847	48780-1	d6a99b39-9991-a426-e053-dadaa90af4c2	Protocoxil

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
71416-001-01	71416000101	45 g in 1 BOTTLE (71416-001-01)	45 g	2017-05-09	0000-00-00	No	No	Current