67777-226 NDC - ZINC OXIDE ()

Drug Information

No.	Package Code	Package Description	Billing Unit
1	67777-226-01	144 PACKET in 1 BOX (67777-226-01) / 5 g in 1 PACKET	GM
2	67777-226-02	36 PACKET in 1 BOX (67777-226-02) / 15 g in 1 PACKET	GM
3	67777-226-03	24 TUBE in 1 CASE (67777-226-03) / 114 g in 1 TUBE	GM
4	67777-226-04	427.5 g in 1 JAR (67777-226-04)	GM

Field Name	Field Value	Definition
PRODUCT NDC	67777-226	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
PROPRIETARY NAME	zinc oxide
START MARKETING DATE	2/1/2011
MARKETING CATEGORY NAME	OTC MONOGRAPH 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	part347	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.
LABELER NAME	Dynarex Corporation	Name of Company corresponding to the labeler code segment of the Product NDC.