FDA.reportPublic FDA data

LACHESIS MUTUS

Manufacturer
SEVENE USA
Effective date
2025-05-22
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:33:40

Label at a glance#

ProductLACHESIS MUTUS 200ck
Active ingredientLACHESIS MUTA VENOM
Label structure12 sections

Dosage and administration

(adults/children) Dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a physician.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

HOMEOPATHIC DILUTION OF HPUS LACHESIS MUTUS 200ck **C,K, CK, AND X ARE HOMEOPATHIC DILUTIONS.

TRADITIONALLY USED FOR

OTC - PURPOSE SECTION

Stinging edemas from stings or allergies, relieved by cold*

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

(adults/children) Dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a physician.

USE

INDICATIONS & USAGE SECTION

Condition listed above or as directed by a physician.

WARNINGS

WARNINGS SECTION

Stop use and ask a physician if symptoms persist for more than 3 days or worsen.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OTHER INFORMATION

OTHER SAFETY INFORMATION

Store at room temperature.

OTC - DO NOT USE SECTION

Do not use if pellet-dispenser seal is broken.

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Sucrose.

QUESTIONS?

OTC - QUESTIONS SECTION

INFO@OLLOIS.COM * www.ollois.com * MADE IN FRANCE. NOT REVIEWED BY THE FDA AND NOT GUARANTEED TO BE EFFECTIVE. THIS HOMEOPATHIC DILUTION MAY NOT BE SUSCEPTIBLE TO SCIENTIFIC MEASUREMENT.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

lachesis 200k p1lachesis 200k p1lachesis 200k p2lachesis 200k p2lachesis 200k p3lachesis 200k p3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76472-3022-12025-02-11C16284748780-12cef2736-87d2-d83d-e063-dadaa90ab31fSevene USA (as PLD) - Lachesis Mutus 200ck (76472-3022)
76472-3022-12025-01-30C16284748780-12cef2736-87d2-d83d-e063-dadaa90ab31fSevene USA (as PLD) - Lachesis Mutus 200ck (76472-3022)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76472-3022-1LACHESIS MUTUS200ck80 in 1 CYLINDERPELLET805

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76472-3022LACHESIS MUTUS 200CK (LACHESIS MUTUS) PELLET [SEVENE USA]5Current NDC, Legacy NDC, 1 package rows20250523_cf85728d-07c8-5a23-e053-2995a90aa6cd.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76472-302276472-3022-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
SUCROSEC151H8M554IACT
LACHESIS MUTA VENOMVSW71SS07IACTIB

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
LACHESIS MUTUS 200ckLACHESIS MUTUSSEVENE USAcf85728d-07c8-5a23-e053-2995a90aa6cd2025-05-22WarningsExact identifier
ndc (package): 76472-3022-1
ndc (product): 76472-3022
ndc11 (package): 76472302201
spl id: 35b7588a-3001-1ce7-e063-6394a90ab714
spl set id: cf85728d-07c8-5a23-e053-2995a90aa6cd

Reported adverse events (FAERS/openFDA)#

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