NDC 0363-9368 Walgreens Flu Relief

Cairina Moschata Heart/liver

NDC Product Code 0363-9368

NDC 0363-9368-31

Package Description: 200 [kp_C] in 1 TUBE

NDC 0363-9368-36

Package Description: 30 TUBE in 1 CARTON > 200 [kp_C] in 1 TUBE

NDC Product Information

Walgreens Flu Relief with NDC 0363-9368 is a a human over the counter drug product labeled by Walgreens Co.. The generic name of Walgreens Flu Relief is cairina moschata heart/liver. The product's dosage form is pellet and is administered via oral form.

Labeler Name: Walgreens Co.

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.

Walgreens Flu Relief 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.

  • CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE 200 [kp_C]/200[kp_C]

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.

  • SUCROSE (UNII: C151H8M554)
  • ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)

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.
  • 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: Walgreens Co.
Labeler Code: 0363
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: 03-01-2020 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: 12-31-2021 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 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Walgreens Flu Relief 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

Otc - Active Ingredient

Anas barbarie 200CK HPUS (10mg)**

Otc - Purpose

Anas barbarie ...... To reduce the duration and severity of flu-like symptoms

Indications & Usage

Temporarily relieves flu-like symptoms such as: body aches, headache, fever, chills, fatigue

Otc - Ask Doctor

Ask a doctor before use in children under 2 years of age.

Otc - Stop Use

Stop use and ask a doctor if symptoms persist for more than 3 days or worsen.

Otc - Pregnancy Or Breast Feeding

If pregnant or breast feeding, ask a health professional before use.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Dosage & Administration

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 day. Children under 2 years of age: Ask a doctor.

Other

Do not use if glued carton and flaps are open or if the tube seal is broken.Each 0.04 oz. dose (1 g) contains 1 g of sugarDissolvable oral pelletsContains 30 Doses

** 200CK is a homeopathic dilution. See www.theaahp.org for more information.
Non-drowsyHomeopathic Medicine**This product is a homeopathic remedy, as such, it has not undergone review or approval by the FDA and therefore has not been demonstrated to be safe or effective to diagnose, treate, prevent, mitigate or cure any condition or disease.††Oscillococcinum is a registered trademark under the patent and trademark act registration number 1305677.

Inactive Ingredient

Lactose, sucrose

Otc - Questions

1-800-264-7661

* Please review the disclaimer below.