58318-003 NDC - ULTRA GLOW FADE ()

Drug Information

No.	Package Code	Package Description	Billing Unit
1	58318-003-01	51 g in 1 CANISTER (58318-003-01)

Field Name	Field Value	Definition
PRODUCT NDC	58318-003	The 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 NAME	Ultra Glow Fade	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
START MARKETING DATE	1/10/2018	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	OTC MONOGRAPH NOT FINAL	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
APPLICATION NUMBER	part358A	The translation of the route code submitted by the firm, indicating route of administration.
LABELER NAME	Keystone Laboratories	Name of Company corresponding to the labeler code segment of the Product NDC.