NDC 0220-2651 Influenzinum

Influenza A Virus A/michigan/45/2015 X-275 (h1n1) Hemagglutinin Antigen (formaldehyde Inactivated), Influenza A Virus A/hong Kong/4801/2014 X-263b (h3n2) Hemagglutinin Antigen (formaldehyde Inactivated), Influenza B Virus B/brisbane/60/2008 Hemagglutinin Antigen (formaldehyde Inactivated)

NDC Product Code 0220-2651

NDC CODE: 0220-2651

Proprietary Name: Influenzinum 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: Influenza A Virus A/michigan/45/2015 X-275 (h1n1) Hemagglutinin Antigen (formaldehyde Inactivated), Influenza A Virus A/hong Kong/4801/2014 X-263b (h3n2) Hemagglutinin Antigen (formaldehyde Inactivated), Influenza B Virus B/brisbane/60/2008 Hemagglutinin Antigen (formaldehyde Inactivated) 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.

Product Characteristics

WHITE (C48325)
Shape: ROUND (C48348)
4 MM

NDC Code Structure

NDC 0220-2651-31

Package Description: 5 PELLET in 1 TUBE

NDC 0220-2651-41

Package Description: 80 PELLET in 1 TUBE

NDC Product Information

Influenzinum with NDC 0220-2651 is a a vaccine lable product labeled by Laboratoires Boiron. The generic name of Influenzinum is influenza a virus a/michigan/45/2015 x-275 (h1n1) hemagglutinin antigen (formaldehyde inactivated), influenza a virus a/hong kong/4801/2014 x-263b (h3n2) hemagglutinin antigen (formaldehyde inactivated), influenza b virus b/brisbane/60/2008 hemagglutinin antigen (formaldehyde inactivated). 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: Vaccine 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.

Influenzinum 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.

  • 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: Laboratoires Boiron
Labeler Code: 0220
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: 03-03-1983 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.

Influenzinum 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 Ingredients

Influenzinum HPUS

8X, 30X, 6C, 9C, 12C, 15C, 30C, 200CK


After-effects of flu or flu-like symptoms*

Stop Use And Ask A Doctor If

Symptoms persist for more than 3 days or worsen.

If Pregnant Or Breast-Feeding,

Ask a health professional before use.


5 pellets 3 times a day until symptoms are relieved.

Other Information

Do not use if pellet dispenser seal is broken.

contains approx. 80 pellets

Inactive Ingredients

Lactose, sucrose


These "Uses" have not been evaluated by the FDA.

* Please review the disclaimer below.