NDC product

up and up hemorrhoidal

NDC 11673-279 · Target Corporation

Key facts

Product NDC 11673-279
Proprietary name up and up hemorrhoidal
Labeler Target Corporation
Marketing category OTC MONOGRAPH DRUG
Application number M015
Marketing start May 23, 2014
Marketing end Nov 30, 2025
Listing certified through Nov 30, 2025

At a glance

  • 1–9 Package NDCs

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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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