78347-102 NDC - OXI WASH ()

Drug Information

Product NDC: 78347-102

Proprietary Name: Oxi Wash

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: BioTek Corporation Inc
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:6/1/2020

Package Information

No. Package Code Package Description Billing Unit
178347-102-0059 mL in 1 BOTTLE, PLASTIC (78347-102-00)
278347-102-01100 mL in 1 BOTTLE, PLASTIC (78347-102-01)
378347-102-03118 mL in 1 BOTTLE, PLASTIC (78347-102-03)
478347-102-04236 mL in 1 BOTTLE, PLASTIC (78347-102-04)
578347-102-05473 mL in 1 BOTTLE, PLASTIC (78347-102-05)
678347-102-063785 mL in 1 BOTTLE, PLASTIC (78347-102-06)

NDC Record

Field Name Field Value Definition
PRODUCT NDC78347-102The 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 NAMEOxi WashThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE6/1/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEBioTek Corporation IncName 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