72483-121 NDC - ALFA HAND SANITIZER ()

Drug Information

Product NDC: 72483-121

Proprietary Name: Alfa Hand Sanitizer

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Laboratorios Alfa SRL
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/30/2020

Package Information

No. Package Code Package Description Billing Unit
172483-121-013840 mL in 1 BOTTLE (72483-121-01)
272483-121-0260 mL in 1 BOTTLE (72483-121-02)
372483-121-04120 mL in 1 BOTTLE (72483-121-04)
472483-121-08240 mL in 1 BOTTLE (72483-121-08)
572483-121-16480 mL in 1 BOTTLE (72483-121-16)

NDC Record

Field Name Field Value Definition
PRODUCT NDC72483-121The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEAlfa Hand SanitizerThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/30/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMELaboratorios Alfa SRLName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 4/12/2024