LACHESIS MUTUS

Manufacturer: REMEDY MAKERS
Effective date: 2011-12-26
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:03:29

Label at a glance#

ProductLACHESIS MUTUS

Active ingredientLACHESIS MUTA VENOM

Label structure8 sections

Contacts and useful links#

Websitewww.remedymakers.com

www.remedymakers.com

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

PMS, CRAMPING, HEADACHE, OR OTHER INDICATIONS

OTC - ACTIVE INGREDIENT SECTION

LACHESIS MUTA VENOM

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

INDICATIONS & USAGE SECTION

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 SECTION

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 SECTION

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 SECTION

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

OTC - QUESTIONS SECTION

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

LACHESISMUTUS6C

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
10191-1457-2	2019-11-13	C162847	48780-1	97449f38-c842-f6ea-e053-dbdaa90aa703	LACHESIS MUTUS 6C (Bushmaster Snake Venom)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
10191-1457-2	LACHESIS MUTUS	143 in 1 VIAL, GLASS	PELLET	143		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
10191-1457	LACHESIS MUTUS (BUSHMASTER VENOM) PELLET [REMEDY MAKERS]	1	Legacy NDC, 1 package rows	20111227_3bd3e350-8f0a-406a-83d4-af4202564508.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version	Uploaded
LACHESIS MUTA VENOM	ACTIVE INGREDIENT	VSW71SS07I	1
LACHESIS MUTA VENOM	ACTIVE MOIETY	VSW71SS07I	1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

LACHESIS MUTUS
BUSHMASTER VENOM
LACHESIS MUTA VENOM
SUCROSE
LACTOSE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
10191-1457	10191-1457-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
LACHESIS MUTA VENOM	VSW71SS07I	ACTIB
SUCROSE	C151H8M554	IACT
LACTOSE	J2B2A4N98G	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
841e844b-e071-4fc9-92a6-794a78dff30d			3bd3e350-8f0a-406a-83d4-af4202564508	2011-12-26	Warnings	Exact identifier spl id: 841e844b-e071-4fc9-92a6-794a78dff30d spl set id: 3bd3e350-8f0a-406a-83d4-af4202564508

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.