NDC 30798-624 - Carolina Custom Cages Chlorhexidine

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: 30798-624
Package NDCs from labels: 30798-624-31, 30798-624-35
Manufacturer: Carolina Designer Dragons, Inc.
Effective date: 2023-05-12
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Chlorhexidine Solution	Carolina Designer Dragons, Inc.	2023-05-12	OTC ANIMAL DRUG LABEL
CHLORHEXIDINE - Durvet \| FIRST PRIORITY INCORPORATED	Durvet \| FIRST PRIORITY INCORPORATED	2019-10-14	OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
30798-624-31	CHLORHEXIDINE	0.473 L in 1 BOTTLE	SOLUTION	0.473	2
30798-624-31	CHLORHEXIDINE	12 in 1 CASE	SOLUTION	12	2
30798-624-35	CHLORHEXIDINE	4 in 1 CASE	SOLUTION	4	2
30798-624-35	CHLORHEXIDINE	3.785 L in 1 JUG	SOLUTION	3.785	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
30798-624	CHLORHEXIDINE SOLUTION [DURVET]	2	4 package rows	20191015_98c833c7-9db4-457a-89fc-6e12fc9292c3.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 9 of 9 · 162 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ANTISEPTIC SKIN CLEANSER	CHLORHEXIDINE GLUCONATE	Xttrium Laboratories, Inc.	6e62eb50-ebaa-361e-e053-2991aa0aba6f	2018-06-11	Warnings	Exact identifier unii: MOR84MUD8E
Hand Wipes	CHLORHEXIDINE DIGLUCONATE AND BENZETHONIUM CHLORIDE	JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.	181e5fa0-ddda-4783-a0b5-ff95bfce6b36	2017-10-09	Warnings	Exact identifier unii: MOR84MUD8E

Reported adverse events (FAERS/openFDA)#

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