FDA.reportPublic FDA data

Arsenicum Album 30C

Manufacturer
Natural Creations, Inc. | OHM Pharma, Inc.
Effective date
2022-02-17
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:16:46

Label at a glance#

ProductArsenicum Album 30C
Active ingredientARSENIC TRIOXIDE
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

​ACTIVE INGREDIENT (HPUS*):

Arsenicum Album 30C

OTC - PURPOSE SECTION

​USES:​ Temporarily relieves upset stomach, nausea, and diarrhea.**

INDICATIONS & USAGE SECTION

​USES:​ Temporarily relieves upset stomach, nausea, and diarrhea.**

DOSAGE & ADMINISTRATION SECTION

​DIRECTIONS:​ Adults & children above 12 years: 10 drops orally 3 times daily, or as directed by a health care professional.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

​KEEP OUT OF THE REACH OF CHILDREN.​ In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away.

WARNINGS SECTION

​WARNINGS:

  • ​Consult a physician for use in children under 12 years of age.
  • IF PREGNANT OR BREAST-FEEDING, ask a health care professional before use.
  • KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away.
  • Do not use if TAMPER EVIDENT seal is broken or missing.

INACTIVE INGREDIENT SECTION

​INACTIVE INGREDIENTS:​ Ethyl Alcohol USP, Purified Water.

OTC - QUESTIONS SECTION

​QUESTIONS & COMMENTS?

Natural Creations, Inc. / Woodbine, IA 51579 / 712-647-1600​

REFERENCES SECTION

​* The letters "HPUS" indicate the component in this product is officially monogrpahed in the Homeopathic Pharmacopeia of the Untied States.

**These statements have not been reviewed by the FDA. They are based on traditional homeopathic practice.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

​NDC: 43406-0168-1

ARSENICUM ALBUM 30C

HOMEOPATHIC

1 fl oz (30 mL) / 20% Alcohol

image descriptionimage description

DailyMed Product Concepts#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43406-0168-12022-02-17C16284748780-1d6a99b39-d3a0-a426-e053-dadaa90af4c2ARSENICUM ALBUM 30C
43406-0168-12022-01-28C16284748780-1d6a99b39-d3a0-a426-e053-dadaa90af4c2ARSENICUM ALBUM 30C

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43406-0168-1Arsenicum Album 30C30 mL in 1 BOTTLE, DROPPERLIQUID303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43406-0168ARSENICUM ALBUM 30C (ARSENIC TRIOXIDE) LIQUID [NATURAL CREATIONS, INC.]3Current NDC, Legacy NDC, 1 package rows20220218_37797a8f-38b9-4007-9d2c-62df4dc92d8a.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
43406-016843406-0168-1

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 TRIOXIDES7V92P67HOACTIM
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

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
Arsenicum Album 30CARSENIC TRIOXIDENatural Creations, Inc.37797a8f-38b9-4007-9d2c-62df4dc92d8a2022-02-17WarningsExact identifier
ndc (package): 43406-0168-1
ndc (product): 43406-0168
ndc11 (package): 43406016801
spl id: c59590ba-6ad8-462f-9ceb-d7cd1b6882f6
spl set id: 37797a8f-38b9-4007-9d2c-62df4dc92d8a

Reported adverse events (FAERS/openFDA)#

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