FDA.reportPublic FDA data

Bestmade Natural Products Crotalus Hor

Manufacturer
Bestmade Natural Products | Total Operations Management LLC DBA: Bestmade Natural Products Micro
Effective date
2025-03-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:32:18

Label at a glance#

ProductBestmade Natural Products Crotalus Hor
Active ingredientCROTALUS HORRIDUS HORRIDUS VENOM
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

How to Use

Take with water 3-4 times a day. Ages 12 or older, 5 Pellets, Ages 12-2, 3 Pellets, Ages below 2, consult your Doctor.

INDICATIONS & USAGE SECTION

Uses

Temporarily supports your body when dealing with outflow, chills, elevated body temperature, loss of appetite, nausea, muscle discomfort, yellowing of the skin and eyes, and related discomfort.*

*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE, NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.

This product is not intended to diagnose, treat, cure, or prevent any disease.

OTC - PURPOSE SECTION

Uses

Temporarily supports your body when dealing with outflow, chills, elevated body temperature, loss of appetite, nausea, muscle discomfort, yellowing of the skin and eyes, and related discomfort.*

*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE, NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.

This product is not intended to diagnose, treat, cure, or prevent any disease.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Crotalus Horridus (Timber Rattlesnake)[HPUS] 30c potency

INACTIVE INGREDIENT SECTION

Ingredients

Inactive: Sucrose/Lactose Pellets base to Preserve Remedy

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Warnings and Storage:

Ask a professional before use if pregnant or breastfeeding or if you have severe symptoms. Keep away from children. If you have a reaction to this product that is not positive, discontinue use. Store in a cool and dry place.

WARNINGS SECTION

Warnings and Storage:

Ask a professional before use if pregnant or breastfeeding or if you have severe symptoms. Keep away from children. If you have a reaction to this product that is not positive, discontinue use. Store in a cool and dry place.

*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE, NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.

This product is not intended to diagnose, treat, cure, or prevent any disease.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Entire package label

crotalus horcrotalus hor

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82969-5047-1Bestmade Natural Products Crotalus Hor30 [hp_C] in 1 BOTTLE, GLASSTABLET, SOLUBLE301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82969-5047BESTMADE NATURAL PRODUCTS CROTALUS HOR (CROTALUS HORRIDUS) TABLET, SOLUBLE [BESTMADE NATURAL PRODUCTS]1Current NDC, 1 package rows20250308_2f973d30-a11b-e082-e063-6294a90a6875.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82969-504782969-5047-1

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
NameUNIIKind
LACTOSEJ2B2A4N98GIACT
CROTALUS HORRIDUS HORRIDUS VENOMYHA2XLJ956ACTIB
SUCROSEC151H8M554IACT

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
Bestmade Natural Products Crotalus HorCROTALUS HORRIDUSBestmade Natural Products2f973d30-a11b-e082-e063-6294a90a68752025-03-05WarningsExact identifier
ndc (package): 82969-5047-1
ndc (product): 82969-5047
ndc11 (package): 82969504701
spl id: 2f973d30-a11c-e082-e063-6294a90a6875
spl set id: 2f973d30-a11b-e082-e063-6294a90a6875

Reported adverse events (FAERS/openFDA)#

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