NDC 68428-319 Cina

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
68428-319
Proprietary Name:
Cina
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Washington Homeopathic Products
Labeler Code:
68428
Start Marketing Date: [9]
02-03-2010
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - WHITE)

Product Packages

NDC Code 68428-319-03

Package Description: 75 PELLET in 1 VIAL, GLASS

NDC Code 68428-319-05

Package Description: 150 PELLET in 1 VIAL, GLASS

NDC Code 68428-319-06

Package Description: 1200 PELLET in 1 BOTTLE, GLASS

NDC Code 68428-319-11

Package Description: 300 PELLET in 1 BOTTLE, GLASS

NDC Code 68428-319-12

Package Description: 600 PELLET in 1 BOTTLE, GLASS

Product Details

What is NDC 68428-319?

The NDC code 68428-319 is assigned by the FDA to the product Cina which is product labeled by Washington Homeopathic Products. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 68428-319-03 75 pellet in 1 vial, glass , 68428-319-05 150 pellet in 1 vial, glass , 68428-319-06 1200 pellet in 1 bottle, glass , 68428-319-11 300 pellet in 1 bottle, glass , 68428-319-12 600 pellet in 1 bottle, glass . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Cina?

Indications:CINA   Worms

Which are Cina UNII Codes?

The UNII codes for the active ingredients in this product are:

  • ARTEMISIA CINA PRE-FLOWERING TOP (UNII: 28M1820ACT)
  • ARTEMISIA CINA PRE-FLOWERING TOP (UNII: 28M1820ACT) (Active Moiety)

Which are Cina Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".