FDA.reportPublic FDA data

NDC 49283-145 - ALFLEXIL ZERO PAIN

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
49283-145
Package NDCs from labels
49283-145-03
Manufacturer
CHEMCO CORPORATION
Effective date
2023-09-14
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
ALFLEXIL ZERO PAIN - CHEMCO CORPORATIONCHEMCO CORPORATION2023-09-14HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49283-145-03ALFLEXIL ZERO PAIN90 g in 1 BOTTLE, WITH APPLICATORGEL901

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49283-145ALFLEXIL ZERO PAIN (CAMPHOR, LIDOCAINE HCL, MENTHOL) GEL [CHEMCO CORPORATION]11 package rows20231019_05574935-31b8-1c4a-e063-6394a90a82cb.zip