FDA.reportPublic FDA data

Arsenicum 6/12/30 Special Order

Manufacturer
Uriel Pharmacy Inc.
Effective date
2018-05-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:09:34

Label at a glance#

ProductArsenicum 6/12/30 Special Order
Active ingredientARSENIC TRIOXIDE
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Use up to every hour. Ages 2 and older: 1-2 sprays. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Arsenicum album (White arsenic) 6X/12X/30X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Distilled water, 30% Organic cane alcohol, Lactose

OTC - PURPOSE SECTION

Uses: Temporary relief of headache.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

WARNINGS SECTION

Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. Contains traces of lactose. If pregnant or nursing, consult a doctor before use. Avoid contact with eyes. Do not use if safety seals on box are broken or missing.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Arsenicum61230SOSprayArsenicum61230SOSpray

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
48951-1291-2Arsenicum 6/12/30 Special Order30 mL in 1 BOTTLE, SPRAYSPRAY301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-1291ARSENICUM 6/12/30 SPECIAL ORDER SPRAY [URIEL PHARMACY INC.]1Legacy NDC, 1 package rows20180503_6b4e86e1-b36f-634a-e053-2a91aa0aeb35.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-129148951-1291-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
ARSENIC TRIOXIDES7V92P67HOACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT
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
6b4e86e1-b370-634a-e053-2a91aa0aeb356b4e86e1-b36f-634a-e053-2a91aa0aeb352018-05-03WarningsExact identifier
spl id: 6b4e86e1-b370-634a-e053-2a91aa0aeb35
spl set id: 6b4e86e1-b36f-634a-e053-2a91aa0aeb35

Reported adverse events (FAERS/openFDA)#

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