Iodine

Manufacturer: Perrigo Direct, Inc | Nice-Pak Products, LLC | Pharma Nobis, LLC
Effective date: 2026-02-19
Label type: HUMAN OTC DRUG LABEL
Version: 13
Source: monthly-update
Hydrated at: 2026-06-03 17:56:41

Label at a glance#

ProductIodine

Active ingredientIODINE, SODIUM IODIDE, ALCOHOL

Label structure13 sections

Dosage and administration

clean the affected area apply a small amount on the area 1 to 3 times daily may be covered with a sterile bandage if bandaged, let dry first

Contacts and useful links#

PhoneLabel contact1-888-593-0593

Websitewww.perrigodriect.com

www.PerrigoDriect.com

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Iodine 2%

Purpose

OTC - PURPOSE SECTION

First aid antiseptic

Use

INDICATIONS & USAGE SECTION

First aid to help prevent skin infection in

minor cuts
scrapes
burns

Warnings

WARNINGS SECTION

For external use only

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

deep or puncture wounds, animal bites or serious burns.

When using this product

OTC - WHEN USING SECTION

do not use in eyes or apply over large areas of the body
do not use longer than 1 week unless directed by a doctor

Stop use and ask a doctor if

OTC - STOP USE SECTION

condition persists or gets worse

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

clean the affected area
apply a small amount on the area 1 to 3 times daily
may be covered with a sterile bandage
if bandaged, let dry first

Other information

SPL UNCLASSIFIED SECTION

product will stain skin and clothing

Inactive ingredients

INACTIVE INGREDIENT SECTION

alcohol (47% v/v), purified water, sodium iodide

ADVERSE REACTION

ADVERSE REACTIONS SECTION

Distributed by: Perrigo Direct, Inc.

Peachtree City, GA 30269

www.PerrigoDriect.com 1-888-593-0593

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 50804-088-10

GoodSense _®

Iodine

Tincture U.S.P.

First Aid Antiseptic

For external use only

CAUTION: POISON

1 FL OZ (30 mL)

image description

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
50804-088-10	2022-11-18	C162847	48780-1	e4f33bdf-b0d2-d8a0-e053-dadaa90a6e4e	Good Sense 088.000/088AA Iodine Tincture USP
50804-088-10	2022-07-29	C162847	48780-1	e4f33bdf-b0d2-d8a0-e053-dadaa90a6e4e	Good Sense 088.000/088AA Iodine Tincture USP

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
50804-088-10	ML - Milliliter	50804-088	4d1d42b1-b184-4786-9d59-ce4ac5fbafef	1	2022-03-09

Products#

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

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

Iodine
WATER
SODIUM IODIDE
IODIDE ION
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
50804-088	50804-088-10

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	ACTIB
SODIUM IODIDE	F5WR8N145C	ACTIM
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
4b30ec52-9ec3-125c-e063-6394a90a1358			3b424440-5bb7-4207-9884-1461a54fbe0b	2026-02-19	Warnings, Adverse reactions	Exact identifier spl id: 4b30ec52-9ec3-125c-e063-6394a90a1358 spl set id: 3b424440-5bb7-4207-9884-1461a54fbe0b

Reported adverse events (FAERS/openFDA)#

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