50544-152 NDC - ACNE WIPEOUT ALL DAY BREAKOUT CONTROL ()

Drug Information

Product NDC: 50544-152

Proprietary Name: ACNE WIPEOUT ALL DAY BREAKOUT CONTROL

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: University Medical Pharmaceuticals Corp.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:6/1/2020

Package Information

No. Package Code Package Description Billing Unit
150544-152-001 TUBE in 1 CARTON (50544-152-00) / 60 mL in 1 TUBE

NDC Record

Field Name Field Value Definition
PRODUCT NDC50544-152The 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 NAMEACNE WIPEOUT ALL DAY BREAKOUT CONTROLThe 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 NAMEUniversity Medical Pharmaceuticals Corp.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