80637-001 NDC - C-TIZERS 99.9 ()

Drug Information

  • Product NDC: 80637-001
  • Proprietary Name: C-tizers 99.9
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: TIZER KOZMETIK LIMITED SIRKETI
Product Type:
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:10/6/2020

Package Information

No. Package Code Package Description Billing Unit
180637-001-011.5 mL in 1 POUCH (80637-001-01)
280637-001-021.5 mL in 1 PACKET (80637-001-02)
380637-001-033 mL in 1 POUCH (80637-001-03)
480637-001-043 mL in 1 PACKET (80637-001-04)
580637-001-0550 mL in 1 BOTTLE (80637-001-05)
680637-001-06100 mL in 1 BOTTLE (80637-001-06)
780637-001-07250 mL in 1 BOTTLE (80637-001-07)
880637-001-08500 mL in 1 BOTTLE (80637-001-08)
980637-001-091000 mL in 1 BOTTLE (80637-001-09)
1080637-001-105000 mL in 1 BOTTLE (80637-001-10)
1180637-001-11150000 mL in 1 DRUM (80637-001-11)
1280637-001-1245 mL in 1 POUCH (80637-001-12)

NDC Record

Field Name Field Value Definition
PRODUCT NDC80637-001The 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 NAMEC-tizers 99.9The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE10/6/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
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 NAMETIZER KOZMETIK LIMITED SIRKETIName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 12/6/2025

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