NDC 71919-201 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:
Proprietary Name:
Product Type: [3]
Labeler Name: [5]
Washington Homeopathic Products
Labeler Code:
Start Marketing Date: [9]
Listing Expiration Date: [11]
Exclude Flag: [12]
Code Navigator:

Product Characteristics

WHITE (C48325 - WHITE)

Product Packages

NDC Code 71919-201-07

Package Description: 15 mL in 1 VIAL, GLASS

NDC Code 71919-201-08

Package Description: 30 mL in 1 VIAL, GLASS

NDC Code 71919-201-09

Package Description: 50 mL in 1 BOTTLE, GLASS

NDC Code 71919-201-10

Package Description: 100 mL in 1 BOTTLE, GLASS

Product Details

What is NDC 71919-201?

The NDC code 71919-201 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 4 packages with assigned NDC codes 71919-201-07 15 ml in 1 vial, glass , 71919-201-08 30 ml in 1 vial, glass , 71919-201-09 50 ml in 1 bottle, glass , 71919-201-10 100 ml 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   Restless sleep

Which are Cina UNII Codes?

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

  • ARTEMISIA CINA FLOWER (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".