NDC 50845-0226 Hemorrhoid Relief

NDC Product Code 50845-0226

NDC 50845-0226-1

Package Description: 30 mL in 1 BOTTLE, SPRAY

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

NDC Product Information

Hemorrhoid Relief with NDC 50845-0226 is a product labeled by Liddell Laboratories, Inc.. The generic name of Hemorrhoid Relief is . The product's dosage form is and is administered via form.

Labeler Name: Liddell Laboratories, Inc.

Dosage Form: -

Product Type: 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.

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.

  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)

Product Labeler Information

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

Labeler Name: Liddell Laboratories, Inc.
Labeler Code: 50845
Start Marketing Date: 11-30-2015 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: 12-31-2020 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 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.

Hemorrhoid Relief Product Label Images

Hemorrhoid 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:

Aesculus Hippocastanum 1X, Arnica Montana 3X, Calcarea Fluorica 9X, Carduus Marianus 1X, Collinsonia Canadensis 3X, Hamamelis Virginiana 3X, Muriaticum Acidum 6X, Ratanhia 3X.

Indications:

May temporarily relieve symptoms associated with hemorrhoids.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

May temporarily relieve symptoms associated with hemorrhoids.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Warnings:

If symptoms persist, consult a doctor.If pregnant or breast feeding, ask a doctor before use.Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away.Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.

Keep Out Of Reach Of Children:

Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away.

Directions:

Adults and children over 12: Spray twice under the tongue 3 times per day.Children 12 and under: Consult a doctor prior to use.

Inactive Ingredients:

Organic alcohol, 23% v/v, Purified water.

Questions:

DIST. BY LIDDELL LABORATORIESWOODBINE, IA 51579WWW.LIDDELL.NET   1-800-460-7733

Package Label Display:

ORAL SPRAYSLIDDELLLABORATORIES27HemHemorrhoidReliefHOMEOPATHIC1.0 FL. OZ. (30 ml)

* Please review the disclaimer below.