NDC product

Cold-EEZE

NDC 61941-0041 · ProPhase Labs, Inc.

Key facts

Product NDC 61941-0041
Proprietary name Cold-EEZE
Labeler ProPhase Labs, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start Feb 1, 2003
Listing certified through Dec 31, 2018

At a glance

  • 1–9 Package NDCs

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About National Drug Codes (NDC)

The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.

Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date:

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