55863-431 NDC - ALCOSCRUB FOAM ()

Drug Information

Product NDC: 55863-431

Proprietary Name: Alcoscrub Foam

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Erie Scientific, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:1/12/2006

Package Information

No. Package Code Package Description Billing Unit
155863-431-0250 mL in 1 BOTTLE (55863-431-02)
255863-431-32950 mL in 1 BOTTLE (55863-431-32)

NDC Record

Field Name Field Value Definition
PRODUCT NDC55863-431The 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 NAMEAlcoscrub FoamThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/12/2006This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEErie Scientific, LLCName 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