79061-042 NDC - PRO CLEAR FOAM ()

Drug Information

Product NDC: 79061-042

Proprietary Name: Pro Clear Foam

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: RELUMINS LABS LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/21/2021

Package Information

No. Package Code Package Description Billing Unit
179061-042-011 BOTTLE in 1 CARTON (79061-042-01) / 60 mL in 1 BOTTLE

NDC Record

Field Name Field Value Definition
PRODUCT NDC79061-042The 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 NAMEPro Clear FoamThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/21/2021This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMERELUMINS LABS LLCName 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