NDC 60512-6669 Eucalyptus Globulus

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  2. Homeolab Usa Inc.
  3. NDC: 60512-6669 Eucalyptus Globulus

NDC Product Code 60512-6669

NDC CODE: 60512-6669

Proprietary Name: Eucalyptus Globulus 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: 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

  • 60512 - Homeolab Usa Inc.

NDC 60512-6669-1

Package Description: 80 PELLET in 1 TUBE

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Eucalyptus Globulus with NDC 60512-6669 is a product labeled by Homeolab Usa Inc.. The generic name of Eucalyptus Globulus is . The product's dosage form is and is administered via form.

Labeler Name: Homeolab Usa Inc.

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 (UNII: J2B2A4N98G)
  • SUCROSE (UNII: C151H8M554)

Product Labeler Information

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

Labeler Name: Homeolab Usa Inc.
Labeler Code: 60512
Start Marketing Date: 11-18-2013 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: 12-31-2019 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: I - INACTIVATED, the listing data was inactivated by the FDA. 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.

Eucalyptus Globulus Product Label Images

Eucalyptus Globulus 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 Hpus

EUCALYPTUS GLOBULUS 1XEucalyptus

Otc - Purpose

COLD AND FLU-LIKE SYMPTOMS*

Use

For self-limiting condition listed above or as directed by a health professional.

Otc - Do Not Use

Do not use if pellet-dispenser seal is broken.

Otc - Stop Use

Stop use and ask a doctor if symptoms persist 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.

Directions

Adults: Allow 3 or 4 pellets to dissolve in the mouth 3 times a day until symptoms are relieved or as directed by a health professional.

Other Information

Store at room temperature.

Inactive Ingredients

Lactose, sucrose.

References

The letters 'HPUS' indicate that the component in this product is officially monographed in the Homeopathic Pharmacopoeia of the United States.*These claims have not been reviewed by the Food and Drug Administration. They are based on traditional homeopathic practice.

Description

80 PelletsPellet dispenserMfd for: HOMEOLAB USA3025 De L'Assomption, Montreal, QC, H1N 2H2, CANADA1-800-404-4666 / www.homeolab.comProduct of Canada

* Please review the disclaimer below.