11822-0779 NDC - BENZETHONIUM CHLORIDE AND DYCLONINE HYDROCHLORIDE ()

Drug Information

Product NDC: 11822-0779

Proprietary Name: Benzethonium Chloride and Dyclonine Hydrochloride

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Rite Aid Corporation
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:2/1/2020

Package Information

No. Package Code Package Description Billing Unit
111822-0779-330 mL in 1 BOTTLE, WITH APPLICATOR (11822-0779-3)

NDC Record

Field Name Field Value Definition
PRODUCT NDC11822-0779The 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 NAMEBenzethonium Chloride and Dyclonine HydrochlorideThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE2/1/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMERite Aid CorporationName 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