NDC 11822-2235 Cairina Moschata Heart/liver Autolysate

Cairina Moschata Heart/liver Autolysate

NDC Product Code 11822-2235

NDC CODE: 11822-2235

Proprietary Name: Cairina Moschata Heart/liver Autolysate What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Cairina Moschata Heart/liver Autolysate What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 11822 - Rite Aid Hdgrts Corp
    • 11822-2235 - Cairina Moschata Heart/liver Autolysate

NDC 11822-2235-3

Package Description: 30 VIAL in 1 CARTON > 200 PELLET in 1 VIAL

NDC Product Information

Cairina Moschata Heart/liver Autolysate with NDC 11822-2235 is a a human over the counter drug product labeled by Rite Aid Hdgrts Corp. The generic name of Cairina Moschata Heart/liver Autolysate is cairina moschata heart/liver autolysate. The product's dosage form is pellet and is administered via oral form.

Dosage Form: Pellet - A small sterile solid mass consisting of a highly purified drug (with or without excipients) made by the formation of granules, or by compression and molding.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Cairina Moschata Heart/liver Autolysate Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.


Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)
  • SUCROSE (UNII: C151H8M554)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

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

Labeler Name: Rite Aid Hdgrts Corp
Labeler Code: 11822
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product 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.

Start Marketing Date: 12-13-2021 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2022 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.

Exclude Flag: N - NO 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".

* Please review the disclaimer below.

Cairina Moschata Heart/liver Autolysate Product Label Images

Cairina Moschata Heart/liver Autolysate Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient                         Purpose

Anas barbariae 200 CK HPUS ............. To reduce the duration and severity of flu-like symptomsThe letters "HPUS" indicate that this ingredient is officially included in the Homeopathic Pharmacopoeia of the United States

Directions

  • Adults and children 2 years of age and older:Dissolve entire contents of one tube in the mouth every 6 hours, up to 3 times a dayChildren under 2 years of age: Ask a doctor.

Other Information

  • Do not use if the tamper evident seal on the flaps is broken or missing or if the tray foil is broken.each 0.04 oz. dose (1g) contains 1 g of sugarstore at 68˚F to 77˚F (20˚C to 25˚C)Questions or comments?Call 1-866-254-3900.Distributed by: RITE AID, 30 HUNTER LANE,CAMP HILL, PA 17011www.riteaid.comMade in India

Inactive Ingredients

Lactose, sucrose

* Please review the disclaimer below.