48951-3210 NDC - CINIS COMP. CI 6 SPECIAL ORDER ()

Drug Information

  • Product NDC: 48951-3210
  • Proprietary Name: Cinis comp. CI 6 Special Order
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Uriel Pharmacy Inc.
Product Type:
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:9/1/2009

Package Information

No. Package Code Package Description Billing Unit
148951-3210-360 mL in 1 BOTTLE, DROPPER (48951-3210-3)

NDC Record

Field Name Field Value Definition
PRODUCT NDC48951-3210Name of Company corresponding to the labeler code segment of the Product NDC.
PROPRIETARY NAMECinis comp. CI 6 Special OrderAn 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.
START MARKETING DATE9/1/2009 
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct 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 NAMEUriel Pharmacy Inc.Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 1/2/2026

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