73893-001 NDC - NOVAGEL HAND SANITIZER ()

Drug Information

Product NDC: 73893-001

Proprietary Name: NovaGel Hand Sanitizer

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: PlasmaDent Inc
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/30/2020

Package Information

No. Package Code Package Description Billing Unit
173893-001-0159.1 mL in 1 BOTTLE, DISPENSING (73893-001-01)
273893-001-02236.6 mL in 1 BOTTLE, DISPENSING (73893-001-02)
373893-001-03473.2 mL in 1 BOTTLE, DISPENSING (73893-001-03)
473893-001-04295.7 mL in 1 BOTTLE, DISPENSING (73893-001-04)
573893-001-05946.4 mL in 1 BOTTLE, DISPENSING (73893-001-05)
673893-001-063800 mL in 1 CONTAINER (73893-001-06)
773893-001-079500 mL in 1 CONTAINER (73893-001-07)
873893-001-0818900 mL in 1 CONTAINER (73893-001-08)
973893-001-09113600 mL in 1 DRUM (73893-001-09)
1073893-001-10189300 mL in 1 DRUM (73893-001-10)
1173893-001-1159.1 mL in 1 TUBE (73893-001-11)
1273893-001-12354.9 mL in 1 BOTTLE, DISPENSING (73893-001-12)

NDC Record

Field Name Field Value Definition
PRODUCT NDC73893-001The 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 NAMENovaGel 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 NAMEPlasmaDent IncName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023