78885-012 NDC - MAGIC XTREME XTRA SOFT ALCOHOL WIPE 1 ()

Drug Information

Product NDC: 78885-012

Proprietary Name: MAGIC XTREME XTRA SOFT ALCOHOL WIPE 1

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	ENSOBRETADOS Y DERIVADOS S.A. DE C.V.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	1/15/2021

No.	Package Code	Package Description	Billing Unit
1	78885-012-00	1 mL in 1 PACKET (78885-012-00)

Field Name	Field Value	Definition
PRODUCT NDC	78885-012	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	MAGIC XTREME XTRA SOFT ALCOHOL WIPE 1	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	1/15/2021	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	ENSOBRETADOS Y DERIVADOS S.A. DE C.V.	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