58831-1001 NDC - EGF UV SHIELD ()

Drug Information

Product NDC: 58831-1001

Proprietary Name: EGF UV SHIELD

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Dermaesthetics Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:6/26/2013

Package Information

No. Package Code Package Description Billing Unit
158831-1001-21 TUBE in 1 BOX (58831-1001-2) / 60 g in 1 TUBE (58831-1001-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC58831-1001The 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 NAMEEGF UV SHIELDThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE6/26/2013This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEDermaesthetics Inc.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