NDC 72127-0707 - Forticept Forteclenz Pro

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 72127-0707
Package NDCs from labels: 72127-0707-1
Manufacturer: Lidan, Inc. | Cosco International, Inc.
Effective date: 2024-09-27
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
FORTICEPT FORTECLENZ PRO ANTIMICROBIAL SHAMPOO	Lidan, Inc. \| Cosco International, Inc.	2024-09-27	OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72127-0707-1	Forticept Forteclenz Pro	.473 kg in 1 BOTTLE, PLASTIC	LIQUID	.473		5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72127-0707	FORTICEPT FORTECLENZ PRO (BENZALKONIUM CHLORIDE) LIQUID [LIDAN, INC.]	5	1 package rows	20240929_f3a589b7-27ee-4d49-a1e4-76b6de825f3f.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 58 of 58 · 1,143 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
CVS Pain Relieving First Aid Antiseptic	LIDOCAINE HYDROCHLORIDE, BENZALKONIUM CHLORIDE	CVS Pharmacy	454b1773-eda8-5610-e054-00144ff88e88	2017-01-04	Warnings	Exact identifier unii: F5UM2KM3W7
CVS Pharmacy Sensitive Medicated Cream	BENZOCAINE, BENZALKONIUM CHLORIDE	CVS Pharmacy	454c3458-7e40-0e5e-e054-00144ff8d46c	2017-01-04	Warnings	Exact identifier unii: F5UM2KM3W7
Sit Clean	BENZALKONIUM CHLORIDE	Sit Clean	ef2b12f8-89b3-47c4-88bd-8712a84cfc45	2016-08-18	Warnings	Exact identifier unii: F5UM2KM3W7

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.