FDA.reportPublic FDA data

Sinusitis Plus

Manufacturer
Deseret Biologicals, Inc. | Apotheca Company
Effective date
2022-11-11
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:48:25

Label at a glance#

ProductSinusitis Plus with ENT Support
Active ingredientPOTASSIUM CHLORIDE, CALCIUM SULFATE ANHYDROUS, SULFUR, MUCOR RACEMOSUS, GOLDENSEAL, POTASSIUM DICHROMATE, LACHESIS MUTA VENOM, MERCURIC SULFIDE, CALCIUM SULFIDE, SILVER NITRATE, COBALT, COPPER, MANGANESE, SILICON DIOXIDE, ASPERGILLUS FUMIGATUS, ASPERGILLUS NIGER VAR. NIGER, CANDIDA ALBICANS, THUJA OCCIDENTALIS LEAFY TWIG, SINUSITISINUM
Label structure9 sections

Dosage and administration

1-10 drops under the tongue, 3 times a day or as directed by a health profressional.  Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION


Kali muriaticum 6X, 200C, Calcarea sulphurica 10X, 200C, Sulphur 6C, Mucor racemousus 6C, 15C, 30C, 200C, Hydrastis canadensis 7C, 200C, Kali bichromicum 7C, 200C, Lachesis mutus 7C, 200C, Mercurius sulphuratus ruber 7C, 200C, Hepar sulphuris calcareum 7C, 10C, 200C, Argentum nitricum 10C, Cobaltum metallicum 10C, Cuprum metallicum 10C, Manganum metallicum 10C, Silicea 10C, Aspergillus fumigatus 10C, 15C, 30C, 200C, Aspergillus niger 10C, 15C, 30C, 200C, Candida albicans 10C, 15C, 30C, 200C, Thuja occidentalis 12C, 200C, Sinusitisinum 15C.

INDICATIONS:

OTC - PURPOSE SECTION

For temporary relief of symptoms related to ear, nose and throat infections including sinus/nasal congestion, cough, and mucous congestion in the middle ear, sneezing, and vaccination reaction.

WARNINGS:

WARNINGS SECTION

Keep out of reach of children.  In case of overdose, contact a physician or Poison Control Center right away.

If pregnant or breast-feeding, ask a health professional before use.

Tamper seal: "Sealed for Your Protection."  Do not use if seal is broken or missing.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.  In case of overdose, contact a physician or Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

1-10 drops under the tongue, 3 times a day or as directed by a health profressional.  Consult a physician for use in children under 12 years of age.

INDICATIONS:

INDICATIONS & USAGE SECTION

For temporary relief of symptoms related to ear, nose and throat infections including sinus/nasal congestion, cough, and mucous congestion in the middle ear, sneezing, and vaccination reaction.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized Water, 25% Ethanol.

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. By: Deseret Biologicals, Inc.

469 Parkland Drive

Sandy, UT 84070     www.desbio.com

PACKAGE LABEL DISPLAY

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DESBIO

NDC 43742-0375-1

HOMEOPATHIC

SINUSITIS PLUS

(with ENT Support)

1 FL OZ (30 ml)

Sinusitis Plus (with ENT Support)Sinusitis Plus (with ENT Support)

Sinusitis Plus (with ENT Support)Sinusitis Plus (with ENT Support)

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43742-0375-12022-11-11C16284748780-19d75b9d0-d36f-f424-e053-dadaa90a57ceDrug Facts
43742-0375-12020-01-31C16284748780-19d75b9d0-d36f-f424-e053-dadaa90a57ceDrug Facts

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ASPERGILLUS FUMIGATUSACTIVE INGREDIENTX88DF51T481
ASPERGILLUS NIGER VAR. NIGERACTIVE INGREDIENT9IOA40ANG61
CALCIUM SULFATE ANHYDROUSACTIVE INGREDIENTE934B3V59H1
CALCIUM SULFIDEACTIVE INGREDIENT1MBW07J51Q1
CANDIDA ALBICANSACTIVE INGREDIENT4D7G21HDBC1
COBALTACTIVE INGREDIENT3G0H8C93621
COPPERACTIVE INGREDIENT789U1901C51
GOLDENSEALACTIVE INGREDIENTZW3Z11D0JV1
LACHESIS MUTA VENOMACTIVE INGREDIENTVSW71SS07I1
MANGANESEACTIVE INGREDIENT42Z2K6ZL8P1
MERCURIC SULFIDEACTIVE INGREDIENTZI0T668SF11
MUCOR RACEMOSUSACTIVE INGREDIENT17RH99LQ7G1
POTASSIUM CHLORIDEACTIVE INGREDIENT660YQ98I101
POTASSIUM DICHROMATEACTIVE INGREDIENTT4423S18FM1
SILICON DIOXIDEACTIVE INGREDIENTETJ7Z6XBU41
SILVER NITRATEACTIVE INGREDIENT95IT3W8JZE1
SINUSITISINUMACTIVE INGREDIENTB575563DM51
SULFURACTIVE INGREDIENT70FD1KFU701
THUJA OCCIDENTALIS LEAFY TWIGACTIVE INGREDIENT1NT28V93971
ASPERGILLUS FUMIGATUSACTIVE MOIETYX88DF51T481
ASPERGILLUS NIGER VAR. NIGERACTIVE MOIETY9IOA40ANG61
CALCIUM CATIONACTIVE MOIETY2M83C4R6ZB1
CALCIUM SULFIDEACTIVE MOIETY1MBW07J51Q1
CANDIDA ALBICANSACTIVE MOIETY4D7G21HDBC1
COBALTACTIVE MOIETY3G0H8C93621
COLLOIDAL SILICON DIOXIDEACTIVE MOIETYETJ7Z6XBU41
COPPERACTIVE MOIETY789U1901C51
DICHROMATE IONACTIVE MOIETY9LKY4BFN2V1
GOLDENSEALACTIVE MOIETYZW3Z11D0JV1
LACHESIS MUTA VENOMACTIVE MOIETYVSW71SS07I1
MANGANESEACTIVE MOIETY42Z2K6ZL8P1
MERCURIC CATIONACTIVE MOIETYED30FJ8Y421
MUCOR RACEMOSUSACTIVE MOIETY17RH99LQ7G1
POTASSIUM CATIONACTIVE MOIETY295O53K1521
SILVER CATIONACTIVE MOIETY57N7B0K90A1
SINUSITISINUMACTIVE MOIETYB575563DM51
SULFURACTIVE MOIETY70FD1KFU701
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 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-037543742-0375-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Name, UNII, Kind table
NameUNIIKind
POTASSIUM CHLORIDE660YQ98I10ACTIM
CALCIUM SULFATE ANHYDROUSE934B3V59HACTIB
SULFUR70FD1KFU70ACTIB
MUCOR RACEMOSUS17RH99LQ7GACTIB
GOLDENSEALZW3Z11D0JVACTIB
POTASSIUM DICHROMATET4423S18FMACTIB
LACHESIS MUTA VENOMVSW71SS07IACTIB
MERCURIC SULFIDEZI0T668SF1ACTIB
CALCIUM SULFIDE1MBW07J51QACTIB
SILVER NITRATE95IT3W8JZEACTIB
COBALT3G0H8C9362ACTIB
COPPER789U1901C5ACTIB
MANGANESE42Z2K6ZL8PACTIB
SILICON DIOXIDEETJ7Z6XBU4ACTIB
ASPERGILLUS FUMIGATUSX88DF51T48ACTIB
ASPERGILLUS NIGER VAR. NIGER9IOA40ANG6ACTIB
CANDIDA ALBICANS4D7G21HDBCACTIB
THUJA OCCIDENTALIS LEAFY TWIG1NT28V9397ACTIB
SINUSITISINUMB575563DM5ACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

Source Document#

Source XML · Source PDF

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 · 59 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALCOHOLALCOHOL3K9958V90MSOLUTION / TRANSDERMAL49.37 %w/vExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSUSPENSION / RECTAL0.35 %v/vExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MGEL / TRANSDERMAL7360 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCONCENTRATE / ORAL198 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MGEL, METERED / TOPICAL541 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSWAB / TOPICAL2250 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MAEROSOL, FOAM / TOPICAL4504 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCONCENTRATE / BUCCAL679 mg/1mlExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MGEL / TOPICAL9971 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE / ORAL882 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSPRAY, METERED / SUBLINGUAL29 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLOTION / TOPICAL25 %w/wExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / INTRAVENOUS400 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MAEROSOL, SPRAY / TOPICAL561 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / DENTAL12.8 %w/wExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / RESPIRATORY (INHALATION)0.08 %w/vExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSPRAY / SUBLINGUAL397 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / INTRAVENOUS99 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MGEL, METERED / TRANSDERMAL3675 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MDROPS / NASAL10 mg/1mlExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MAEROSOL, SPRAY / RESPIRATORY (INHALATION)35.75 %w/wExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MELIXIR / ORAL13675 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MTABLET, DELAYED RELEASE / ORALNAExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MINJECTION / SUBCUTANEOUS149 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MINJECTION / INTRAVASCULAR100 %v/vExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MINJECTION / INTRAMUSCULAR1491 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / OPHTHALMIC0.5 %w/vExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MAEROSOL / TOPICAL561 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSPRAY / TRANSDERMAL90 %w/vExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / ORAL6624 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MAEROSOL, METERED / NASAL70 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSUSPENSION / ORAL681 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MGEL / DENTAL1.8 %w/wExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MINJECTION / INTRAVENOUS92 %w/vExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSHAMPOO / TOPICAL714 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MPOWDER, FOR SOLUTION / TOPICAL40 %w/wExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MINJECTION, SOLUTION / INTRAVENOUS6405 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MJELLY / VAGINALNAExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSPRAY / NASAL20 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MAEROSOL, METERED / RESPIRATORY (INHALATION)26664 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION, CONCENTRATE / INTRAVENOUS4000 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MPASTE / DENTAL1.8 %w/wExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MGEL / RECTAL898 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSPRAY / TOPICAL3633 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSYRUP / ORAL21000 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / NASAL10 mg/1mlExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MINJECTION, SOLUTION / INTRAMUSCULAR1000 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / INTRAMUSCULAR400 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / INTRAVESICAL7892 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MINJECTION, SOLUTION / SUBCUTANEOUS6.1 %v/vExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE, EXTENDED RELEASE / ORAL8 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / RESPIRATORY (INHALATION)5 %w/wExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MINJECTION, EMULSION / INTRAVENOUS520 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MMOUTHWASH / BUCCAL200 mg/1mlExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MDROPS / ORAL210 mg/1mlExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MAEROSOL / NASAL20 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / TOPICAL2445 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION, CONCENTRATE / ORAL150.68 mg/1mlExact identifier — unii candidate
59 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
2d951f19-8720-4a2a-aeb7-c39658a72580ecacdc80-d53b-474f-a561-a172a6ba704d2022-11-11WarningsExact identifier
spl id: 2d951f19-8720-4a2a-aeb7-c39658a72580
spl set id: ecacdc80-d53b-474f-a561-a172a6ba704d

Reported adverse events (FAERS/openFDA)#

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