71788-016 NDC - FOAMING CHLORHEXIDINE GLUCONATE ()

Drug Information

Product NDC: 71788-016

Proprietary Name: Foaming Chlorhexidine Gluconate

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

No.	Package Code	Package Description
1	71788-016-20	4 BOTTLE, PUMP in 1 CARTON (71788-016-20) / 1000 mL in 1 BOTTLE, PUMP (71788-016-10)
2	71788-016-60	12 BOTTLE, PUMP in 1 CARTON (71788-016-60) / 530 mL in 1 BOTTLE, PUMP (71788-016-50)
3	71788-016-80	24 BOTTLE, PUMP in 1 CARTON (71788-016-80) / 100 mL in 1 BOTTLE, PUMP (71788-016-70)

Field Name	Field Value	Definition
PRODUCT NDC	71788-016	The 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 NAME	Foaming Chlorhexidine Gluconate	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	4/13/2021	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Protect U Guard, LLC	Name 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