FDA.reportPublic FDA data

SINUS HP

Manufacturer
Natural Creations, Inc. | OHM Pharma, Inc.
Effective date
2025-12-16
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:36:01

Label at a glance#

ProductSINUS HP
Active ingredientAMBROSIA ARTEMISIIFOLIA, ARSENIC TRIOXIDE, CALCIUM SULFIDE, POTASSIUM DICHROMATE, POTASSIUM SULFATE, LYCOPODIUM CLAVATUM SPORE, MERCURIUS SOLUBILIS, SODIUM CHLORIDE, PHOSPHORUS, PULSATILLA VULGARIS, SEPIA OFFICINALIS JUICE, SILICON DIOXIDE, THUJA OCCIDENTALIS LEAFY TWIG
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS (HPUS*) equal amounts of: Ambrosia 30C, Arsenicum Album 30C, Hepar Sulphuris Calcareum 30C, Kali Bichromicum 30C, Kali Sulphuricum 30C, Lycopodium Clavatum 30C, Mercurius Solubilis 30C, Natrum Muriaticum 30C, Phosphorus 30C, Pulsatilla 30C, Sepia 30C, Silicea 30C, Thuja Occidentalis 30C.

INDICATIONS & USAGE SECTION

USES: Temporarily relieves watery, runny nose, obstructed nose, post nasal drip, sinus congestion, sinus headache, and/or symptoms related to a sinus infection.**

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.

* 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 health 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 watery, runny nose, obstructed nose, post nasal drip, sinus congestion, sinus headache, and/or symptoms related to a sinus infection.**

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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 43406-0045-1

SINUS HP

HOMEOPATHIC

1 fl oz (30 mL) / 20% Alcohol

UPC: 877730000330

image descriptionimage description

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130877730000330GTIN-13: 0877730000330
EAN-13: 0877730000330
GTIN-12: 877730000330
UPC-A: 877730000330
GTIN storage (14 digits): 00877730000330		SINUS HP.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
bed0530e-f939-4541-956b-6928a2f6404fProduct name120241008
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name620240814
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name220171212
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43406-0045-12023-01-19C16284748780-19855d018-ee1f-cd31-e053-dbdaa90ab51aSINUS HP
43406-0045-12019-11-27C16284748780-19855d018-ee1f-cd31-e053-dbdaa90ab51aSINUS HP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43406-0045-1SINUS HP30 mL in 1 BOTTLE, DROPPERLIQUID304

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AMBROSIA ARTEMISIIFOLIAACTIVE INGREDIENT9W34L2CQ9A1
ARSENIC TRIOXIDEACTIVE INGREDIENTS7V92P67HO1
CALCIUM SULFIDEACTIVE INGREDIENT1MBW07J51Q1
LYCOPODIUM CLAVATUM SPOREACTIVE INGREDIENTC88X29Y4791
MERCURIUS SOLUBILISACTIVE INGREDIENT324Y4038G21
PHOSPHORUSACTIVE INGREDIENT27YLU75U4W1
POTASSIUM DICHROMATEACTIVE INGREDIENTT4423S18FM1
POTASSIUM SULFATEACTIVE INGREDIENT1K573LC5TV1
PULSATILLA VULGARISACTIVE INGREDIENTI76KB35JEV1
SEPIA OFFICINALIS JUICEACTIVE INGREDIENTQDL83WN8C21
SILICON DIOXIDEACTIVE INGREDIENTETJ7Z6XBU41
SODIUM CHLORIDEACTIVE INGREDIENT451W47IQ8X1
THUJA OCCIDENTALIS LEAFY TWIGACTIVE INGREDIENT1NT28V93971
AMBROSIA ARTEMISIIFOLIAACTIVE MOIETY9W34L2CQ9A1
ARSENIC CATION (3)ACTIVE MOIETYC96613F5AV1
CALCIUM SULFIDEACTIVE MOIETY1MBW07J51Q1
CHLORIDE IONACTIVE MOIETYQ32ZN486981
COLLOIDAL SILICON DIOXIDEACTIVE MOIETYETJ7Z6XBU41
DICHROMATE IONACTIVE MOIETY9LKY4BFN2V1
LYCOPODIUM CLAVATUM SPOREACTIVE MOIETYC88X29Y4791
MERCURIUS SOLUBILISACTIVE MOIETY324Y4038G21
PHOSPHORUSACTIVE MOIETY27YLU75U4W1
PULSATILLA VULGARISACTIVE MOIETYI76KB35JEV1
SEPIA OFFICINALIS JUICEACTIVE MOIETYQDL83WN8C21
SULFATE IONACTIVE MOIETY7IS9N8KPMG1
THUJA OCCIDENTALIS LEAFY TWIGACTIVE MOIETY1NT28V93971
ALCOHOLINACTIVE INGREDIENT3K9958V90M1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43406-004543406-0045-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
AMBROSIA ARTEMISIIFOLIA9W34L2CQ9AACTIB
ARSENIC TRIOXIDES7V92P67HOACTIB
CALCIUM SULFIDE1MBW07J51QACTIB
POTASSIUM DICHROMATET4423S18FMACTIB
POTASSIUM SULFATE1K573LC5TVACTIB
LYCOPODIUM CLAVATUM SPOREC88X29Y479ACTIB
MERCURIUS SOLUBILIS324Y4038G2ACTIB
SODIUM CHLORIDE451W47IQ8XACTIB
PHOSPHORUS27YLU75U4WACTIB
PULSATILLA VULGARISI76KB35JEVACTIB
SEPIA OFFICINALIS JUICEQDL83WN8C2ACTIB
SILICON DIOXIDEETJ7Z6XBU4ACTIB
THUJA OCCIDENTALIS LEAFY TWIG1NT28V9397ACTIB
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
SINUS HPAMBROSIA ARTEMISIIFOLIA, ARSENIC TRIOXIDE, CALCIUM SULFIDE, POTASSIUM DICHROMATE, POTASSIUM SULFATE, LYCOPODIUM CLAVATUM SPORE, MERCURIUS SOLUBILIS, SODIUM CHLORIDE, PHOSPHORUS, PULSATILLA VULGARIS, SEPIA OFFICINALIS JUICE, SILICON DIOXIDE, THUJA OCCIDENTALIS LEAFY TWIGNatural Creations, Inc.f017da22-74c2-40f4-adcc-5e84b6ea52912025-12-16WarningsExact identifier
ndc (package): 43406-0045-1
ndc (product): 43406-0045
ndc11 (package): 43406004501
spl id: cede75c3-53de-4822-a5fc-a804c1b22a05
spl set id: f017da22-74c2-40f4-adcc-5e84b6ea5291

Reported adverse events (FAERS/openFDA)#

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