NDC 62106-6870 Muco Coccinum

Klebsiella Pneumoniae

NDC Product Code 62106-6870

NDC CODE: 62106-6870

Proprietary Name: Muco Coccinum 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: Klebsiella Pneumoniae 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

Color(s):
WHITE (C48325)
Shape: ROUND (C48348)
Size(s):
9 MM
Score: 1

NDC Code Structure

  • 62106 - Seroyal Usa

NDC 62106-6870-0

Package Description: 1 BLISTER PACK in 1 BOX > 10 TABLET in 1 BLISTER PACK

NDC Product Information

Muco Coccinum with NDC 62106-6870 is a a human over the counter drug product labeled by Seroyal Usa. The generic name of Muco Coccinum is klebsiella pneumoniae. The product's dosage form is tablet and is administered via sublingual form.

Labeler Name: Seroyal Usa

Dosage Form: Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.

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.

Muco Coccinum 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.

  • ANAEROCOCCUS TETRADIUS 200 [hp_C]/1
  • INFLUENZA A VIRUS 200 [hp_C]/1
  • INFLUENZA B VIRUS 200 [hp_C]/1
  • KLEBSIELLA PNEUMONIAE 200 [hp_C]/1
  • MORAXELLA CATARRHALIS SUBSP. CATARRHALIS 200 [hp_C]/1

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.

  • CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
  • LACTOSE (UNII: J2B2A4N98G)
  • MAGNESIUM STEARATE (UNII: 70097M6I30)
  • XYLITOL (UNII: VCQ006KQ1E)

Administration Route(s)

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

  • Sublingual - Administration beneath the tongue.

Product Labeler Information

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

Labeler Name: Seroyal Usa
Labeler Code: 62106
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: 10-15-2014 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.

Muco Coccinum Product Label Images

Muco Coccinum 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

Active ingredientsEach tablet contains:

Branhamella catarrhalis 200K

Influenzinum 200K

Klebsiella pneumoniae 200K

Micrococcus tetragenus 200K

Otc - Purpose

UsesFor the temporary relief of cold and flu-like symptoms

Warnings

Warnings

This product is not intended to be an alternative to

vaccination.

Do not use if you have ever had an allergic reaction to this

product or any of its ingredients.

Stop use and ask a doctor if symptoms continue to persist

after three days of use or are accompanied by a fever.

If pregnant or breastfeeding, ask a health professional before

use. Keep out of reach of children. In case of overdose, get

medical help or contact a Poison Control Center right away.

Otc - Do Not Use

Do not use if you have ever had an allergic reaction to this product or any of its ingredients.

Otc - Pregnancy Or Breast Feeding

If pregnant or breastfeeding, ask a health professional before use.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Overdosage

In case of overdose, get medical help or contact a Poison Control Center right away.

Inactive Ingredient

Inactive ingredientsCarboxymethylcellulose sodium, lactose monohydrate (milk), magnesium stearate, xylitol

Other Safety Information

Other information

Do not use if the blister pack has been tampered with.

Store in a cool, dry place.

Dosage & Administration

Directions

Adults and Adolescents (12 years and older): At the first sign of symptoms, take one tablet allowing it to dissolve under the tongue. If

symptoms persist, take one tablet two or three times during the day or as recommended by your healthcare practitioner.
Children (6-11 years): Take under the direction of your healthcare practitioner.

Indications & Usage

UsesFor the temporary relief of cold and flu-like symptoms.Directions

Adults and Adolescents (12 years and older): At the first sign of symptoms, take one tablet allowing it to dissolve under the tongue. If

symptoms persist, take one tablet two or three times during the day or as recommended by your healthcare practitioner.
Children (6-11 years): Take under the direction of your healthcare practitioner.

* Please review the disclaimer below.