78279-001 NDC - PANION AND BF HAND SANITIZER ()

Drug Information

  • Product NDC: 78279-001
  • Proprietary Name: PANION AND BF Hand Sanitizer
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: PANION & BF BIOTECH INC.
Product Type:
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:6/30/2020

Package Information

No. Package Code Package Description Billing Unit
178279-001-18120 mL in 1 BOTTLE (78279-001-18)
278279-001-23300 mL in 1 BOTTLE (78279-001-23)
378279-001-28500 mL in 1 BOTTLE (78279-001-28)
478279-001-301000 mL in 1 BOTTLE (78279-001-30)
578279-001-323785 mL in 1 BOTTLE (78279-001-32)
678279-001-35360 mL in 1 BOTTLE (78279-001-35)
778279-001-49225 mL in 1 BOTTLE (78279-001-49)
878279-001-99240 mL in 1 BOTTLE (78279-001-99)

NDC Record

Field Name Field Value Definition
PRODUCT NDC78279-001Product 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.
PROPRIETARY NAMEPANION AND BF Hand SanitizerThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
START MARKETING DATE6/30/2020Name of Company corresponding to the labeler code segment of the Product NDC.
MARKETING CATEGORY NAMEOTC MONOGRAPH NOT FINALProduct 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 NUMBERpart333AThis 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 NAMEPANION & BF BIOTECH INC.Name of Company corresponding to the labeler code segment of the Product NDC.

Download Record

Download this NDC record record in Text format: Export

Download this NDC record record in Excel (CSV) format: Export

Download this NDC record record in XML format: Export

This page was last updated on: 1/16/2026

Previous Code
Next Code