Iodine

Manufacturer: United Natural Foods, Inc. dba UNFI | Nice-Pak Products, LLC | Pharma Nobis
Effective date: 2026-02-16
Label type: HUMAN OTC DRUG LABEL
Version: 18
Source: full-release
Hydrated at: 2026-06-01 01:46:11

Label at a glance#

ProductIodine

Active ingredientIODINE

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 contact1-877-932-7948

Websitewww.supervalu-ourownbrands.com

www.supervalu-ourownbrands.com

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Iodine tincture U.S.P. 100% (2% iodine)

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Not Listed: alcohol (47% v/v), purified water, sodium iodide

Other information

SPL UNCLASSIFIED SECTION

Product will stain skin and clothing

SPL UNCLASSIFIED SECTION

Distributed by UNFI, Eden Prairie, MN 55344 USA

Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 41163-088-10

EQUALINE

iodine tincture USP

first aid antiseptic

for external use only

CAUTION POISON

1 OZ (30 mL)

image description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
311093	iodine 2 % Topical Solution	PSN	18
311093	iodine 20 MG/ML Topical Solution	SCD	18
311093	iodine 2 % tincture for Topical Solution	SY	18
311093	iodine 2 % Topical Solution	SY	18

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
41163-088-10	2022-09-30	C162847	48780-1	e4f33bdf-b007-d8a0-e053-dadaa90a6e4e	Equaline 088.000/088AA Iodine Tincture U.S.P.
41163-088-10	2022-07-29	C162847	48780-1	e4f33bdf-b007-d8a0-e053-dadaa90a6e4e	Equaline 088.000/088AA Iodine Tincture U.S.P.

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
41163-088-10	Iodine	30 mL in 1 BOTTLE, PLASTIC	LIQUID	30		18

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
ALCOHOL	ACTIVE INGREDIENT	3K9958V90M	1
IODINE	ACTIVE INGREDIENT	9679TC07X4	1
SODIUM IODIDE	ACTIVE INGREDIENT	F5WR8N145C	1
ALCOHOL	ACTIVE MOIETY	3K9958V90M	1
IODIDE ION	ACTIVE MOIETY	09G4I6V86Q	1
IODINE	ACTIVE MOIETY	9679TC07X4	1
water	INACTIVE INGREDIENT	059QF0KO0R	1

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Iodine
ALCOHOL
WATER
SODIUM IODIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
41163-088	41163-088-10

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
ALCOHOL	3K9958V90M	IACT
WATER	059QF0KO0R	IACT
SODIUM IODIDE	F5WR8N145C	IACT
IODINE	9679TC07X4	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
Iodine	IODINE	United Natural Foods, Inc. dba UNFI	8e840855-d210-4a99-b73f-6c69dcf2b6fb	2026-02-16	Warnings	Exact identifier ndc (package): 41163-088-10 ndc (product): 41163-088 ndc11 (package): 41163008810 spl id: 4af729f3-e20c-e7e0-e063-6294a90aca80 spl set id: 8e840855-d210-4a99-b73f-6c69dcf2b6fb

Reported adverse events (FAERS/openFDA)#

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