NDC 10191-1457 Lachesis Mutus
NDC Product 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.
Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
NDC Code Structure
- 10191 - Remedy Makers
- 10191-1457 - Lachesis Mutus
NDC 10191-1457-2
Package Description: 143 PELLET in 1 VIAL, GLASS
NDC Product Information
Lachesis Mutus with NDC 10191-1457 is a product labeled by Remedy Makers. The generic name of Lachesis Mutus is . The product's dosage form is and is administered via form.
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.
- 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 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.
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
- Otc - Active Ingredient
- Otc - Keep Out Of Reach Of Children
- Indications & Usage
- Warnings
- Dosage & Administration
- Inactive Ingredient
- Otc - Questions
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.