57520-0654 NDC - SINUS RESCUE ()

Drug Information

No.	Package Code	Package Description	Billing Unit
1	57520-0654-1	30 mL in 1 BOTTLE, DROPPER (57520-0654-1)

Field Name	Field Value	Definition
PRODUCT NDC	57520-0654	This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
PROPRIETARY NAME	Sinus Rescue	Name of Company corresponding to the labeler code segment of the Product NDC.
PROPRIETARY NAME SUFFIX	1	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
START MARKETING DATE	3/31/2011	The translation of the dosage form Code submitted by the firm.
MARKETING CATEGORY NAME	UNAPPROVED HOMEOPATHIC	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.
LABELER NAME	Apotheca Company	Name of Company corresponding to the labeler code segment of the Product NDC.