NDC 13985-222 - Lidocaine 2%

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
13985-222
Package NDCs from labels
13985-222-04, 13985-222-05
Manufacturer
MWI/VetOne
Effective date
2020-02-14
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Lidocaine 2% - MWI/VetOneMWI/VetOne2020-02-14PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
13985-222-04Lidocaine2%100 mL in 1 BOTTLEINJECTION1004
13985-222-05Lidocaine2%250 mL in 1 BOTTLEINJECTION2504

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
13985-222LIDOCAINE 2% (LIDOCAINE) INJECTION [MWI/VETONE]42 package rows20200215_84d4dc99-daaa-41e5-9da9-25c7922e285f.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
LIDOCAINE HYDROCHLORIDEACTIVE INGREDIENTV13007Z41ALIDOCAINE 2% (LIDOCAINE) INJECTION [MWI/VETONE]2
LIDOCAINEACTIVE MOIETY98PI200987LIDOCAINE 2% (LIDOCAINE) INJECTION [MWI/VETONE]2

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 34 of 34 · 662 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
First Aid BurnBENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDEWater-Jel Technologies25ebf112-8ac3-4402-9a87-00e454ab7efa2017-11-30WarningsExact identifier
unii: V13007Z41A
CVS Pain Relieving First Aid AntisepticLIDOCAINE HYDROCHLORIDE, BENZALKONIUM CHLORIDECVS Pharmacy454b1773-eda8-5610-e054-00144ff88e882017-01-04WarningsExact identifier
unii: V13007Z41A

Reported adverse events (FAERS/openFDA)#

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