22431-227 NDC - URBAN STREET OCEAN BREEZE ()

Drug Information

Product NDC: 22431-227

Proprietary Name: Urban Street Ocean Breeze

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Blue Cross Laboratories LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:7/19/2021

Package Information

No. Package Code Package Description Billing Unit
122431-227-019.6 g in 1 TUBE (22431-227-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC22431-227The 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 NAMEUrban Street Ocean BreezeThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE7/19/2021This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEBlue Cross Laboratories LLCName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 4/12/2024