4TP - ORAL SOLUTION (82926-204)

Manufacturer
4TP LLC
Effective date
2022-10-04
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:51:17

Label at a glance#

Product4TP ORAL
Active ingredientZINC IODIDE
Label structure9 sections

Indications and uses

RELIEVES RESPIRATORY DIFFICULTIES & BRONCHIAL IRRITATIONS (COUGH).

Dosage and administration

Shake well before use. Mix liquid as detailed below into a glass of water or juice. Adults and children 13 years and older (up to 120lbs): 5ml, three times daily For heavier body weight or very severe cases dose 10ml, three times daily

Storage and handling

STORE AT ROOM TEMPERATURE AWAY FROM DIRECT LIGHT. DOES NOT REQUIRE REFRIGERATION.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ZINCUM IODATUM 2X HPUS

PURPOSE

OTC - PURPOSE SECTION

TO TREAT RESPIRATORY DIFFICULTIES, COUGH AND PERTUSSIS

USES

INDICATIONS & USAGE SECTION

RELIEVES RESPIRATORY DIFFICULTIES & BRONCHIAL IRRITATIONS (COUGH).

WARNINGS

WARNINGS SECTION

WHEN USING THIS PRODUCT

  • If pregnant or breast-feeding, ask a healthcare professional before use
  • Children under 12: consult a doctor before use
  • Do not exceed recommended dosage
  • The use of this container by more than one person may spread infection
  • For your safety do not use if seal is broken

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control center right away

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Shake well before use.

Mix liquid as detailed below into a glass of water or juice.

  • Adults and children 13 years and older (up to 120lbs): 5ml, three times daily
  • For heavier body weight or very severe cases dose 10ml, three times daily

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

DMSO, WATER

OTHER INFORMATION

STORAGE AND HANDLING SECTION

STORE AT ROOM TEMPERATURE AWAY FROM DIRECT LIGHT.

DOES NOT REQUIRE REFRIGERATION.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_4TP_Oral Liquid_5mL01b LBL_4TP_Oral Liquid_5mL

01b LBL_4TP_Oral Liquid_100mL01b LBL_4TP_Oral Liquid_100mL

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82926-20482926-204-11, 82926-204-51, 82926-204-21, 82926-204-52

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIMETHYL SULFOXIDEYOW8V9698HIACT
WATER059QF0KO0RIACT
ZINC IODIDE762R7A0O0BACTIM

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
f66db5c8-ceaa-38df-e053-2995a90a8bede56e8d41-188e-5a6f-e053-2a95a90a70e62023-03-08WarningsExact identifier
spl set id: e56e8d41-188e-5a6f-e053-2a95a90a70e6

Reported adverse events (FAERS/openFDA)#

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