FDA.reportPublic FDA data

Allergy HP

Manufacturer
Natural Creations, Inc. | OHM Pharma, Inc.
Effective date
2022-02-17
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:37:21

Label at a glance#

ProductAllergy HP
Active ingredientONION, AMBROSIA ARTEMISIIFOLIA, ARSENIC TRIOXIDE, ACTIVATED CHARCOAL, EUPHRASIA STRICTA, STRYCHNOS NUX-VOMICA SEED, PULSATILLA VULGARIS, SOLIDAGO VIRGAUREA FLOWERING TOP, SULFUR
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients (HPUS*): Allium Cepa 30C, Ambrosia Artemisiifolia 30C, Arsenicum Album 30C, Carbo Vegetabilis 30C, Euphrasia Officinalis 30C, Nux Vomica 30C, Phosphorus 30C, Pulsatilla 30C, Solidago Virgaurea 30C, Sulfur 30C

INDICATIONS & USAGE SECTION

USES: Temporarily relieves hay fever, coryza, itching & burning eyes, coughing &/or other symptoms associated with hay fever & allergies.**

WARNINGS SECTION

WARNING:

  • Consult a physician for use in children under 12 years of age. 
  • IF PREGNANT OR BREAST-FEEDING, ask a health 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.

DOSAGE & ADMINISTRATION SECTION

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

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: Ethyl Alcohol USP, Purified Water.

OTC - QUESTIONS SECTION

QUESTIONS AND COMMENTS?

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

OTC - PURPOSE SECTION

USES: Temporarily relieves hay fever, coryza, itching & burning eyes, coughing &/or other symptoms associated with hay fever & allergies.**

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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 43406-0002-1

ALLERGY HP

HOMEOPATHIC

1 fl oz (30 mL) / 20% Alcohol

UPC: 87730000378

image descriptionimage description

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130877730000378GTIN-13: 0877730000378
EAN-13: 0877730000378
GTIN-12: 877730000378
UPC-A: 877730000378
GTIN storage (14 digits): 00877730000378		Allergy HP.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43406-0002-12022-02-17C16284748780-197449f38-bae0-f6ea-e053-dbdaa90aa703Allergy HP
43406-0002-12022-02-17C16284748780-197449f38-bae0-f6ea-e053-dbdaa90aa703Allergy HP
43406-0002-12022-01-28C16284748780-197449f38-bae0-f6ea-e053-dbdaa90aa703Allergy HP
43406-0002-12022-01-28C16284748780-197449f38-bae0-f6ea-e053-dbdaa90aa703Allergy HP
43406-0002-12020-01-04C16284748780-197449f38-bae0-f6ea-e053-dbdaa90aa703Allergy HP
43406-0002-12020-01-04C16284748780-197449f38-bae0-f6ea-e053-dbdaa90aa703Allergy HP
43406-0002-12019-11-13C16284748780-197449f38-bae0-f6ea-e053-dbdaa90aa703Allergy HP
43406-0002-12019-11-13C16284748780-197449f38-bae0-f6ea-e053-dbdaa90aa703Allergy HP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43406-0002-1Allergy HP30 mL in 1 BOTTLE, DROPPERLIQUID304

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ACTIVATED CHARCOALACTIVE INGREDIENT2P3VWU3H101
AMBROSIA ARTEMISIIFOLIAACTIVE INGREDIENT9W34L2CQ9A1
ARSENIC TRIOXIDEACTIVE INGREDIENTS7V92P67HO1
EUPHRASIA STRICTAACTIVE INGREDIENTC9642I91WL1
ONIONACTIVE INGREDIENT492225Q21H1
PULSATILLA VULGARISACTIVE INGREDIENTI76KB35JEV1
SOLIDAGO VIRGAUREA FLOWERING TOPACTIVE INGREDIENT5405K23S501
STRYCHNOS NUX-VOMICA SEEDACTIVE INGREDIENT269XH139191
SULFURACTIVE INGREDIENT70FD1KFU701
ACTIVATED CHARCOALACTIVE MOIETY2P3VWU3H101
AMBROSIA ARTEMISIIFOLIAACTIVE MOIETY9W34L2CQ9A1
ARSENIC CATION (3+)ACTIVE MOIETYC96613F5AV1
EUPHRASIA STRICTAACTIVE MOIETYC9642I91WL1
ONIONACTIVE MOIETY492225Q21H1
PULSATILLA VULGARISACTIVE MOIETYI76KB35JEV1
SOLIDAGO VIRGAUREA FLOWERING TOPACTIVE MOIETY5405K23S501
STRYCHNOS NUX-VOMICA SEEDACTIVE MOIETY269XH139191
SULFURACTIVE MOIETY70FD1KFU701
ALCOHOLINACTIVE INGREDIENT3K9958V90M1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43406-000243406-0002-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
ONION492225Q21HACTIB
AMBROSIA ARTEMISIIFOLIA9W34L2CQ9AACTIB
ARSENIC TRIOXIDES7V92P67HOACTIB
ACTIVATED CHARCOAL2P3VWU3H10ACTIB
EUPHRASIA STRICTAC9642I91WLACTIB
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB
PULSATILLA VULGARISI76KB35JEVACTIB
SOLIDAGO VIRGAUREA FLOWERING TOP5405K23S50ACTIB
SULFUR70FD1KFU70ACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
32022-02-17full-release2026-06-01 02:16:45

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
Allergy HPONION, AMBROSIA ARTEMISIIFOLIA, ARSENIC TRIOXIDE, ACTIVATED CHARCOAL, EUPHRASIA STRICTA, STRYCHNOS NUX-VOMICA SEED, PULSATILLA VULGARIS, SOLIDAGO VIRGAUREA FLOWERING TOP, SULFURNatural Creations, Inc.0d374e26-6a25-44d4-8133-6c4b0be8e4112022-02-17WarningsExact identifier
ndc (package): 43406-0002-1
ndc (product): 43406-0002
ndc11 (package): 43406000201
spl id: 771837a9-f933-4eb3-bcf4-9bcc4f880396
spl set id: 0d374e26-6a25-44d4-8133-6c4b0be8e411

Reported adverse events (FAERS/openFDA)#

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