FDA.reportPublic FDA data

Bestmade Natural Products Arsenicum Album

Manufacturer
Bestmade Natural Products | Total Operations Management LLC DBA: Bestmade Natural Products Micro
Effective date
2025-05-27
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:33:45

Label at a glance#

ProductBestmade Natural Products Arsenicum Album
Active ingredientARSENIC TRIOXIDE
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 in recovery from digestive upset and vomiting.*

*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.

INACTIVE INGREDIENT SECTION

Ingredients

Inactive: Sucrose/Lactose Pellets base to Preserve Remedy

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Arsenicum Album (Arsenic Trioxide) [HPUS] 30c potency

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.

OTC - PURPOSE SECTION

Uses

Temporarily supports your body in recovery from digestive upset and vomiting.*

*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.

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

arsenicumarsenicum

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82969-5016-1Bestmade Natural Products Arsenicum Album30 [hp_C] in 1 BOTTLE, GLASSTABLET, SOLUBLE302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82969-5016BESTMADE NATURAL PRODUCTS ARSENICUM ALBUM (ARSENICUM ALBUM) TABLET, SOLUBLE [BESTMADE NATURAL PRODUCTS]21 package rows20250529_29a1a224-9a6a-31a1-e063-6294a90a9e18.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82969-501682969-5016-1

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
ARSENIC TRIOXIDES7V92P67HOACTIB
SUCROSEC151H8M554IACT
LACTOSE, UNSPECIFIED FORMJ2B2A4N98GIACT

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 Arsenicum AlbumARSENICUM ALBUMBestmade Natural Products29a1a224-9a6a-31a1-e063-6294a90a9e182025-05-27WarningsExact identifier
ndc (package): 82969-5016-1
ndc (product): 82969-5016
ndc11 (package): 82969501601
spl id: 3620a51e-9a58-2d80-e063-6294a90a5a82
spl set id: 29a1a224-9a6a-31a1-e063-6294a90a9e18

Reported adverse events (FAERS/openFDA)#

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