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.

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 - 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.

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.