41250-551 NDC - MEDICATED BODY POWDER ()

Drug Information

Product NDC: 41250-551

Proprietary Name: Medicated Body Powder

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Meijer Distribution, Inc
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/5/2009

Package Information

No. Package Code Package Description Billing Unit
141250-551-38.283 kg in 1 BOTTLE, PUMP (41250-551-38)

NDC Record

Field Name Field Value Definition
PRODUCT NDC41250-551The 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 NAMEMedicated Body PowderThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/5/2009This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEMeijer Distribution, 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