FDA.reportPublic FDA data

TinitX

Manufacturer
Deseret Biologicals, Inc. | Apotheca Company
Effective date
2021-07-30
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:14:46

Label at a glance#

ProductTinitX
Active ingredientONION, SILVER NITRATE, DYSPHANIA AMBROSIOIDES WHOLE, SOLANUM DULCAMARA TOP, GINKGO, QUININE SULFATE, SUS SCROFA CARTILAGE, SUS SCROFA NASAL MUCOSA, ASARUM CANADENSE ROOT, ONOSMODIUM VIRGINIANUM, SODIUM SALICYLATE, ACTIVATED CHARCOAL, CARBON DISULFIDE, CYCLAMEN PURPURASCENS TUBER, GOSSYPIUM HERBACEUM ROOT BARK, GRAPHITE, WOOD CREOSOTE, PHOSPHORUS, LEAD, THERIDION CURASSAVICUM, ZINC
Label structure9 sections

Dosage and administration

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

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Allium Cepa 6X, Argentum Nitricum 6X, Chenopodium Anthelminticum 6X, Dulcamara 6X, Ginkgo Biloba 6X, Chininum Sulphuricum 6X, 12X, 30X, 200X, Cartilago Suis 8X, 12X, 30X, 200X, Mucosa Nasalis Suis 8X, 12X, 30X, 200X, Asarum Canadense 9X, Onosmodium Virginianum 10X, Natrum Salicylicum 10X, 12X, 30X, 200X, Carbo Vegetabilis 12X, Carboneum Sulphuratum 12X, Cyclamen Europaeum 12X, Gossypium Herbaceum 12X, Graphites 12X, Kreosotum 12X, Phosphorus 12X, Plumbum Metallicum 12X, Theridion 12X, Zincum Metallicum 12X.

HOMEOPATHIC INDICATIONS:

OTC - PURPOSE SECTION

For the temporary relief of symptoms related to tinnitus, such as noises in ear following injury, decreased hearing, sensitivity to noise, noises with motion .**

**These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

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 professional. Consult a physician for use in children under 12 years of age.

HOMEOPATHIC INDICATIONS:

INDICATIONS & USAGE SECTION

For the temporary relief of symptoms related to tinnitus, such as noises in ear following injury, decreased hearing, sensitivity to noise, noises with motion .**

**These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized Water, 25% Ethanol

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. By: Deseret Biologicals, Inc.

469 W. Parkland Drive

Sandy, UT 84070 www.desbio.com

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DESBIO

NDC 43742-1646-1

HOMEOPATHIC

TinitX

1 FL OZ (30 ml)

TinitXTinitX

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
22bca8fc-c2b1-897d-b515-117a7522ccaeProduct name320150731
6cca4355-1206-91f7-02de-17eef38a8622Product name120140508
751c581a-bf64-2fd7-b3ec-ca02c83e4a00Product name120140508

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43742-1646TINITX (ALLIUM CEPA, ARGENTUM NITRICUM, CHENOPODIUM ANTHELMINTICUM, DULCAMARA, GINKGO BILOBA, CHININUM SULPHURICUM, CARTILAGO SUIS, MUCOSA NASALIS SUIS, ASARUM CANADENSE, ONOSMODIUM VIRGINIANUM, NATRUM SALICYLICUM, CARBO VEGETABILIS, CARBONEUM SULPHURATUM, CYCLAMEN EUROPAEUM, GOSSYPIUM HERBACEUM, GRAPHITES, KREOSOTUM, PHOSPHORUS, PLUMBUM METALLICUM, THERIDION, ZINCUM METALLICUM) LIQUID [DESERET BIOLOGICALS, INC.]2Legacy NDC20210731_5ba07aec-9ade-403a-9415-a87328558b82.zip

Products#

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

DailyMed product names page 1 of 1 · 29 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-164643742-1646-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 matching rows.

Name, UNII, Kind table
NameUNIIKind
ONION492225Q21HACTIB
SILVER NITRATE95IT3W8JZEACTIB
DYSPHANIA AMBROSIOIDES WHOLE4H5RSU087IACTIB
SOLANUM DULCAMARA TOPKPS1B1162NACTIB
GINKGO19FUJ2C58TACTIB
QUININE SULFATEKF7Z0E0Q2BACTIB
SUS SCROFA CARTILAGE73ECW5WG2FACTIB
SUS SCROFA NASAL MUCOSAID3Z1X61WYACTIB
ASARUM CANADENSE ROOTE2O4O7TQYKACTIB
ONOSMODIUM VIRGINIANUM604NK4250SACTIB
SODIUM SALICYLATEWIQ1H85SYPACTIB
ACTIVATED CHARCOAL2P3VWU3H10ACTIB
CARBON DISULFIDES54S8B99E8ACTIB
CYCLAMEN PURPURASCENS TUBERG728143D8QACTIB
GOSSYPIUM HERBACEUM ROOT BARKVQN1631P4CACTIB
GRAPHITE4QQN74LH4OACTIB
WOOD CREOSOTE3JYG22FD73ACTIB
PHOSPHORUS27YLU75U4WACTIB
LEAD2P299V784PACTIB
THERIDION CURASSAVICUM9Z8D3HEM8LACTIB
ZINCJ41CSQ7QDSACTIB
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
65c8fd27-99d4-42dc-9108-f3442df82afb5ba07aec-9ade-403a-9415-a87328558b822021-07-30WarningsExact identifier
spl id: 65c8fd27-99d4-42dc-9108-f3442df82afb
spl set id: 5ba07aec-9ade-403a-9415-a87328558b82

Reported adverse events (FAERS/openFDA)#

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