NDC 10191-1457 Lachesis Mutus

Product Information

What is NDC 10191-1457?

The NDC code 10191-1457 is assigned by the FDA to the product Lachesis Mutus which is product labeled by Remedy Makers. The product's dosage form is and is administered via form. The product is distributed in a single package with assigned NDC code 10191-1457-2 143 pellet in 1 vial, glass . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information, RxNorm crosswalk and the complete product label.

NDC Product Code10191-1457
Proprietary Name 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.
Lachesis Mutus
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Remedy Makers
Labeler Code10191
Start Marketing Date 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 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 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".
NDC Code Structure

What are the uses for Lachesis Mutus?

Product Packages

NDC Code 10191-1457-2

Package Description: 143 PELLET in 1 VIAL, GLASS

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

Product Details

Lachesis Mutus Active Ingredients UNII Codes

Lachesis Mutus Inactive Ingredients UNII Codes

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.

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Lachesis Mutus Product Label

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Label Table of Contents

Otc - Purpose


Otc - Active Ingredient


Otc - Keep Out Of Reach Of Children

WARNING:Keep this and all medications out of reach of children.

Indications & Usage

INDICATIONS: To be use according to standard homeopathic indications, for self-limiting conditions such as these indicated above or as directed by a physician.


WARNING: Use only if cap and seal are unbroken. If symptoms persist for more than 3 days or worsen, discontinue (STOP) use and consult your physician. As with any drug. If you are pregnant or nursing (breast-feeding) a baby, seek the advise of a health professional before using this product. Store tightly closed in a cool area.

Dosage & Administration

Directions:(adult/children) Dissolve 3 or 4 pellets in mouth or under tongue 3 times a day or as directed by a physician. Children 2 years and older take 1/2 the adult dose.

Inactive Ingredient

Inactive Ingredient: Lactose and Sucrose. Free from yeast, wheat, corn and soy.

Otc - Questions

Questions or comments.(877)REM4YOU. Fax (909)594-4205 Pomona, CA. 91768. USA www.remedymakers.com

Other information: Contain approx.143 - 151 pellets.

Package Label.Principal Display Panel

* Please review the disclaimer below.