Strong Iodine Tincture

Manufacturer: Humo Holding Group, Inc. | Humco Holding Group, Inc.
Effective date: 2017-11-09
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:52:56

Label at a glance#

ProductStrong Iodine Tincture

Active ingredientALCOHOL

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 Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 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

Iodine 7%, Potassium Iodide 5%, Purified water

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
5f30b278-5791-4113-8781-878a9221ef8a	Product name	2	20230125
2a70c781-a755-4d76-b20a-a958acfbdcdc	Product name	2	20190619
304592ef-4a8a-4c22-8e8c-af73aa3d60e5	Product name	1	20180703
ac0821a1-ce75-4ea7-880a-59eecaecdf22	Product name	1	20180703
db5dc4f9-b907-46f6-8fb7-babcf04bbe5c	Product name	1	20180619
41e9d6cf-3ed7-4c44-a57e-0685058d0896	Product name	1	20170824
5e652c92-68fd-426b-b0e7-5fc64e0b9f99	Product name	1	20170309
ddc0c11a-bba8-408f-b3c7-c4828b4bcc8c	Product name	1	20150421

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
0395-1220-16	2022-07-29	C162847	48780-1	e4f33bdf-a72a-d8a0-e053-dadaa90a6e4e	Humco Strong Iodine Tincture
0395-1220-91	2022-07-29	C162847	48780-1	e4f33bdf-a72a-d8a0-e053-dadaa90a6e4e	Humco Strong Iodine Tincture

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0395-1220-16	Strong Iodine Tincture	473 mL in 1 BOTTLE, PLASTIC	LIQUID	473		1
0395-1220-91	Strong Iodine Tincture	30 mL in 1 BOTTLE, PLASTIC	LIQUID	30		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0395-1220	STRONG IODINE TINCTURE (IODINE TINCTURE) LIQUID [HUMO HOLDING GROUP, INC.]	1	Legacy NDC, 2 package rows	20171110_5d93562d-f6af-c699-e053-2a91aa0aec3b.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

Strong Iodine Tincture
Iodine Tincture
WATER
IODINE
POTASSIUM IODIDE
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
0395-1220	0395-1220-16, 0395-1220-91

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
Name	UNII	Kind
WATER	059QF0KO0R	IACT
IODINE	9679TC07X4	IACT
POTASSIUM IODIDE	1C4QK22F9J	IACT
ALCOHOL	3K9958V90M	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
5d9340bf-91fc-7f15-e053-2a91aa0a1195			5d93562d-f6af-c699-e053-2a91aa0aec3b	2017-11-09	Warnings	Exact identifier spl id: 5d9340bf-91fc-7f15-e053-2a91aa0a1195 spl set id: 5d93562d-f6af-c699-e053-2a91aa0aec3b

Reported adverse events (FAERS/openFDA)#

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