71788-001 NDC - PROTECT U GUARD ANTIBACTERIAL FOAMING ()

Drug Information

Product NDC: 71788-001

Proprietary Name: Protect U Guard Antibacterial Foaming

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Protect U Guard, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:6/3/2020

Package Information

No. Package Code Package Description Billing Unit
171788-001-204 BOTTLE, DISPENSING in 1 CARTON (71788-001-20) / 1000 mL in 1 BOTTLE, DISPENSING (71788-001-10)
271788-001-6012 BOTTLE in 1 CARTON (71788-001-60) / 530 mL in 1 BOTTLE (71788-001-50)

NDC Record

Field Name Field Value Definition
PRODUCT NDC71788-001The 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 NAMEProtect U Guard Antibacterial FoamingThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE6/3/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEProtect U Guard, 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