NDC 29983-0010 - BLUE RIBBON

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
29983-0010
Package NDCs from labels
29983-0010-1, 29983-0010-4, 29983-0010-6, 29983-0010-7, 29983-0010-8
Manufacturer
IBA
Effective date
2022-07-19
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
BLUE RIBBON - IBAIBA2022-07-19OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
29983-0010-1BLUE RIBBON3.78 L in 1 DRUMSOLUTION3.782
29983-0010-4BLUE RIBBON18.9 L in 1 DRUMSOLUTION18.92
29983-0010-6BLUE RIBBON56.7 L in 1 DRUMSOLUTION56.72
29983-0010-7BLUE RIBBON113.4 L in 1 DRUMSOLUTION113.42
29983-0010-8BLUE RIBBON207.9 L in 1 DRUMSOLUTION207.92

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
29983-0010BLUE RIBBON (CHLORHEXIDINE GLUCONATE) SOLUTION [IBA]25 package rows20220721_15864f64-2f86-4f7b-8a01-6154717af8ef.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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ANTISEPTIC SKIN CLEANSERCHLORHEXIDINE GLUCONATEXttrium Laboratories, Inc.6e62eb50-ebaa-361e-e053-2991aa0aba6f2018-06-11WarningsExact identifier
unii: MOR84MUD8E
Hand WipesCHLORHEXIDINE DIGLUCONATE AND BENZETHONIUM CHLORIDEJIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.181e5fa0-ddda-4783-a0b5-ff95bfce6b362017-10-09WarningsExact identifier
unii: MOR84MUD8E

Reported adverse events (FAERS/openFDA)#

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