NDC 10191-1457 Lachesis Mutus

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  3. NDC: 10191-1457 Lachesis Mutus

NDC Product Code 10191-1457

NDC CODE: 10191-1457

Proprietary Name: Lachesis Mutus 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

  • 10191 - Remedy Makers

NDC 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.

NDC Product Information

Lachesis Mutus with NDC 10191-1457 is a product labeled by Remedy Makers. 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: Remedy Makers
Labeler Code: 10191
Start Marketing Date: 10-31-2006 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: 12-31-2017 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.

Lachesis Mutus Product Label Images

Lachesis Mutus 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

Otc - Purpose

PMS, CRAMPING, HEADACHE, OR OTHER INDICATIONS

Otc - Active Ingredient

LACHESIS MUTA VENOM

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.

Warnings

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.comOther information: Contain approx.143 - 151 pellets.

* Please review the disclaimer below.