FDA.reportPublic FDA data

Arthritis HP

Manufacturer
Natural Creations, Inc. | OHM Pharma, Inc.
Effective date
2025-11-13
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:35:10

Label at a glance#

ProductArthritis HP
Active ingredientAPIS MELLIFERA, BRYONIA ALBA ROOT, CAUSTICUM, KALMIA LATIFOLIA LEAF, LEDUM PALUSTRE TWIG, PULSATILLA VULGARIS, RHODODENDRON AUREUM LEAF, TOXICODENDRON PUBESCENS LEAF
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients (HPUS*): Apis Mellifica 30X, Bryonia Alba 30X, Causticum 30X, Colchicum Autumnale 30X, Kalmia Latifolia 30X, Ledum Palustre 30X, Pulsatilla 30X, Rhododendron Chrysanthum 30X, Rhus Toxicodendron 30X

INDICATIONS & USAGE SECTION

USES: Temporarily relief of minor arthritis pain.**

WARNINGS SECTION

WARNING:

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.

DOSAGE & ADMINISTRATION SECTION

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

OTC - DO NOT USE SECTION

OTHER INFORMATION: Tamper Seal: "Sealed for your protection."

Do not use if seal is broken or missing.

REFERENCES SECTION

*The letters "HPUS" indicate the components in the product are officially monographed in the Homeopathic Pharmacopeia of the United States.

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: Purified Water, USP Ethanol Alcohol 20%

OTC - QUESTIONS SECTION

QUESTIONS AND COMMENTS?

Natural Creations / Woodbine, IA 51579 / 712-647-1600

OTC - PURPOSE SECTION

USES: Temporarily relief of minor arthritis pain.**

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 43406-0005-1

ARTHRITIS HP

HOMEOPATHIC

1 fl oz (30 mL) / 20% Alcohol

Image Of LabelImage Of Label

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130877730000408GTIN-13: 0877730000408
EAN-13: 0877730000408
GTIN-12: 877730000408
UPC-A: 877730000408
GTIN storage (14 digits): 00877730000408		Arthritis HP.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43406-0005-12023-01-19C16284748780-19855d018-e543-cd31-e053-dbdaa90ab51aArthritis HP
43406-0005-12019-11-27C16284748780-19855d018-e543-cd31-e053-dbdaa90ab51aArthritis HP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43406-0005-1Arthritis HP30 mL in 1 BOTTLE, DROPPERLIQUID303

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
APIS MELLIFERAACTIVE INGREDIENT7S82P3R43Z1
BRYONIA ALBA ROOTACTIVE INGREDIENTT7J046YI2B1
CAUSTICUMACTIVE INGREDIENTDD5FO1WKFU1
KALMIA LATIFOLIA LEAFACTIVE INGREDIENT79N6542N181
LEDUM PALUSTRE TWIGACTIVE INGREDIENT877L01IZ0P1
PULSATILLA VULGARISACTIVE INGREDIENTI76KB35JEV1
RHODODENDRON AUREUM LEAFACTIVE INGREDIENTIV92NQJ73U1
TOXICODENDRON PUBESCENS LEAFACTIVE INGREDIENT6IO182RP7A1
APIS MELLIFERAACTIVE MOIETY7S82P3R43Z1
BRYONIA ALBA ROOTACTIVE MOIETYT7J046YI2B1
CAUSTICUMACTIVE MOIETYDD5FO1WKFU1
KALMIA LATIFOLIA LEAFACTIVE MOIETY79N6542N181
LEDUM PALUSTRE TWIGACTIVE MOIETY877L01IZ0P1
PULSATILLA VULGARISACTIVE MOIETYI76KB35JEV1
RHODODENDRON AUREUM LEAFACTIVE MOIETYIV92NQJ73U1
TOXICODENDRON PUBESCENS LEAFACTIVE MOIETY6IO182RP7A1
ALCOHOLINACTIVE INGREDIENT3K9958V90M1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43406-000543406-0005-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
APIS MELLIFERA7S82P3R43ZACTIB
BRYONIA ALBA ROOTT7J046YI2BACTIB
CAUSTICUMDD5FO1WKFUACTIB
KALMIA LATIFOLIA LEAF79N6542N18ACTIB
LEDUM PALUSTRE TWIG877L01IZ0PACTIB
PULSATILLA VULGARISI76KB35JEVACTIB
RHODODENDRON AUREUM LEAFIV92NQJ73UACTIB
TOXICODENDRON PUBESCENS LEAF6IO182RP7AACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates

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
Arthritis HPAPIS MELLIFERA, BRYONIA ALBA ROOT, CAUSTICUM, COLCHICUM AUTUMNALE BULB, KALMIA LATIFOLIA LEAF, LEDUM PALUSTRE TWIG, PULSATILLA VULGARIS, RHODODENRON AUREUM LEAF, TOXICODENDREN PUBESCENS LEAFNatural Creations, Inc.3455dda6-4329-443b-8322-0b11ce7414432025-11-13WarningsExact identifier
ndc (package): 43406-0005-1
ndc (product): 43406-0005
ndc11 (package): 43406000501
spl id: 268640e5-30ad-45c8-816d-2565d3fa3c8d
spl set id: 3455dda6-4329-443b-8322-0b11ce741443

Reported adverse events (FAERS/openFDA)#

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