FDA.reportPublic FDA data

Humco Strong Iodine Tincture

Manufacturer
Humo Holding Group, Inc. | Humco Holding Group, Inc.
Effective date
2020-06-21
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:24:52

Label at a glance#

ProductHumco Strong Iodine Tincture
Active ingredientIODINE, POTASSIUM IODIDE, ALCOHOL
Label structure12 sections

Indications and uses

To prevent infection in mior cuts, scrapes, and burns.

Dosage and administration

Clean affacted area Apply a small amount on the area 1 to 3 times daily. May be covered with sterile bandage. If bandaged, let it dry first.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Iodine 7%

Potassium Iodide 5%

alcohl 85%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

To prevent infection in mior cuts, scrapes, and burns.

Warnings

WARNINGS SECTION

For external use only

Ask a doctor if you have:

OTC - ASK DOCTOR SECTION

deep or puncture wounds

animal bites

serious burns.

Stop use and consult a doctor if:

OTC - STOP USE SECTION

The condition persists or gets worse, or if using for longer than once a week.

When using this product:

OTC - WHEN USING SECTION

Do not use in the eyes. If contact occurs, flush with large amounts of water lifting upper and lower lids.

do not apply over large areas of the body.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, give milk then a starch solution made by mixing two tablespoonfuls of cornstarch or flour to a pint of water. contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Clean affacted area

Apply a small amount on the area 1 to 3 times daily.

May be covered with sterile bandage.

If bandaged, let it dry first.

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Purified water

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Strong.jpgStrong.jpgimage descriptionimage description

Label

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0395-1219-16ML - Milliliter0395-12194d80c46e-f75d-46fa-becf-6ce1be8744a012014-04-03
0395-1219-91ML - Milliliter0395-12196b626e75-7f5f-4c92-a77a-671fdadf4b3a12017-12-14

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ALCOHOLACTIVE INGREDIENT3K9958V90M1
IODINEACTIVE INGREDIENT9679TC07X41
POTASSIUM IODIDEACTIVE INGREDIENT1C4QK22F9J1
ALCOHOLACTIVE MOIETY3K9958V90M1
IODIDE IONACTIVE MOIETY09G4I6V86Q1
IODINEACTIVE MOIETY9679TC07X41
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0395-12190395-1219-16, 0395-1219-91

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
IODINE9679TC07X4ACTIB
POTASSIUM IODIDE1C4QK22F9JACTIM
ALCOHOL3K9958V90MACTIB

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
da6bcd14-2286-e7df-e053-2995a90a45265835e005-4721-4ec1-98e8-412aba4e19f02022-03-17WarningsExact identifier
spl set id: 5835e005-4721-4ec1-98e8-412aba4e19f0

Reported adverse events (FAERS/openFDA)#

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