FDA.reportPublic FDA data

4TP - 50mg/Capsule (82926-101)

Manufacturer
4TP LLC
Effective date
2022-08-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:52:28

Label at a glance#

Product4TP
Active ingredientZINC IODIDE
Label structure9 sections

Indications and uses

Relieves respiratory difficulties and bronchial irritations (cough).

Dosage and administration

Adults and children up to 13 years: Take 1 capsule three times daily for weight up to 120lbs. For heavier body weight or more severe cases, take 2 capsules three times

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ZINCUM IODATUM 50 MG

PURPOSE

OTC - PURPOSE SECTION

TO TREAT RESPIRATORY DIFFICULTIES, COUGH AND PERTUSSIS

USES

INDICATIONS & USAGE SECTION

Relieves respiratory difficulties and bronchial irritations (cough).

WARNINGS

WARNINGS SECTION

  • Children under 12: consult a doctor before using
  • Do not use if the blister seal is broken
  • If pregnant or breast-feeding ask a healthcare professional before use
  • Store in a cool, dry place, away from direct light.

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

  • Adults and children up to 13 years: Take 1 capsule three times daily for weight up to 120lbs.
  • For heavier body weight or more severe cases, take 2 capsules three times

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

NAC (N-acetyl cysteine), magnesium stearate

OTHER INGREDIENTS: BOVINE GELATIN, GLYCERIN, PURIFIED WATER, TITANIUM DIOXIDE

QUESTIONS

OTC - QUESTIONS SECTION

CALL TOLL FREE 1-800-XXX-XXXX

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_4TP_Capsules_60ct01b LBL_4TP_Capsules_60ct

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82926-10182926-101-60

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
ACETYLCYSTEINEWYQ7N0BPYCIACT
MAGNESIUM STEARATE70097M6I30IACT
GELATIN, UNSPECIFIED2G86QN327LIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
ZINC IODIDE762R7A0O0BACTIB

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
f66df23f-3c2e-12e5-e053-2a95a90aad55e56ed39d-030e-5bb0-e053-2995a90ac02f2023-03-08WarningsExact identifier
spl set id: e56ed39d-030e-5bb0-e053-2995a90ac02f

Reported adverse events (FAERS/openFDA)#

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