NDC 60512-9059 Hemorrhoids Relief

  1. Labeler Index
  2. Homeolab Usa Inc.
  3. NDC: 60512-9059 Hemorrhoids Relief

NDC Product Code 60512-9059

NDC CODE: 60512-9059

Proprietary Name: Hemorrhoids Relief 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.

NDC Code Structure

  • 60512 - Homeolab Usa Inc.

NDC 60512-9059-1

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

Hemorrhoids Relief with NDC 60512-9059 is a product labeled by Homeolab Usa Inc.. The product's dosage form is and is administered via form.

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)
  • LACTOSE (UNII: J2B2A4N98G)

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: 10-18-2013 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.

Hemorrhoids Relief Product Label Images

Hemorrhoids 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

Active Ingredients Hpus

Aesculus hippocastanum 1XHamamelis virginiana 1XPaeonia officinalis 3XCollinsonia 3XTeucrium marum 3XVerbascum thapsus 3XBoldo 1XSulphur 4XSodium nitrate 3XRatanhia 3XAcidum nitricum 8XNatrum muriaticum 8XPodophyllum peltatum 4XRuta graveolens 8XApis mellifica 4X

References

Manufactured according to the Homeopathic Pharmacopoeia of the United States (HPUS)

Purpose

Helps relieve discomfort of hemorrhoids and fissures

Uses

This Homeopathic product of natural source helps relieve the discomfort and pain caused by hemorrhoids and fissures.

Otc - Ask Doctor

If symptoms persist or worsen, discontinue use and contact a health professional.

Otc - Pregnancy Or Breast Feeding

As with any drug, if you are pregnant or nursing a baby, seek the advice of a health professional before using this product.

Otc - Keep Out Of Reach Of Children

Keep this and all medications out of reach of children.

Directions

Adults: Allow 3 pellets to dissolve under the tongue 3 times a day, or as directed by a health professional.For adult use only. Do not exceed recommended dosage.

Other Information

Do not use if cap seal is broken.Homeolab USA Inc., 3025 De L'Assomption Blvd., Montreal, QC H1N 2H2  CanadaPRODUCT OF CANADA

* Please review the disclaimer below.