NDC 17856-0799 - MYLICON

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
17856-0799
Package NDCs from labels
17856-0799-1, 17856-0799-2, 17856-0799-3, 17856-0799-4, 17856-0799-5
Manufacturer
ATLANTIC BIOLOGICALS CORP. | UNIT DOSE SOLUTIONS
Effective date
2023-05-16
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
MYLICON - ATLANTIC BIOLOGICALS CORP. | UNIT DOSE SOLUTIONSATLANTIC BIOLOGICALS CORP. | UNIT DOSE SOLUTIONS2023-05-16HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17856-0799-1MYLICON0.3 mL in 1 SYRINGESUSPENSION0.35
17856-0799-1MYLICON120 in 1 BOX, UNIT-DOSESUSPENSION1205
17856-0799-2MYLICON0.3 mL in 1 SYRINGESUSPENSION0.35
17856-0799-2MYLICON120 in 1 BOX, UNIT-DOSESUSPENSION1205
17856-0799-3MYLICON120 in 1 BOX, UNIT-DOSESUSPENSION1205
17856-0799-3MYLICON0.6 mL in 1 SYRINGESUSPENSION0.65
17856-0799-4MYLICON0.6 mL in 1 SYRINGESUSPENSION0.65
17856-0799-4MYLICON120 in 1 BOX, UNIT-DOSESUSPENSION1205
17856-0799-5MYLICON1.2 mL in 1 SYRINGESUSPENSION1.25
17856-0799-5MYLICON60 in 1 BOX, UNIT-DOSESUSPENSION605

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17856-0799MYLICON (SIMETHICONE) SUSPENSION [ATLANTIC BIOLOGICALS CORP.]510 package rows20230517_e47eca0a-4678-4c72-97f0-144e6aa06520.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
17856-0799-2EA - Each17856-07996231fff9-6087-44e2-b869-95ac1f053ff412024-01-04
17856-0799-3EA - Each17856-0799fbb331c3-c318-4d75-87cf-f9a495d5411412023-10-16