52000-025 NDC - HYDROGEN PEROXIDE ()

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Drug Information

Product NDC: 52000-025

Proprietary Name: Hydrogen Peroxide

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	Universal Distribution Center LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	11/25/2015

No.	Package Code	Package Description
1	52000-025-03	237 mL in 1 BOTTLE, PLASTIC (52000-025-03)
2	52000-025-06	414 mL in 1 BOTTLE, PLASTIC (52000-025-06)
3	52000-025-07	473 mL in 1 BOTTLE, PLASTIC (52000-025-07)
4	52000-025-31	295 mL in 1 BOTTLE, PLASTIC (52000-025-31)
5	52000-025-32	354 mL in 1 BOTTLE, PLASTIC (52000-025-32)
6	52000-025-40	100 mL in 1 BOTTLE, PLASTIC (52000-025-40)
7	52000-025-41	119 mL in 1 BOTTLE, PLASTIC (52000-025-41)
8	52000-025-42	178 mL in 1 BOTTLE, PLASTIC (52000-025-42)
9	52000-025-43	200 mL in 1 BOTTLE, PLASTIC (52000-025-43)
10	52000-025-44	250 mL in 1 BOTTLE, PLASTIC (52000-025-44)
11	52000-025-45	266 mL in 1 BOTTLE, PLASTIC (52000-025-45)

Field Name	Field Value	Definition
PRODUCT NDC	52000-025	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	Hydrogen Peroxide	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	11/25/2015	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Universal Distribution Center 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