Iodine by UNFI / Vi-Jon, LLC / Pharma Nobis IODINE liquid

Iodine by

Drug Labeling and Warnings

Iodine by is a Otc medication manufactured, distributed, or labeled by UNFI, Vi-Jon, LLC, Pharma Nobis. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Iodine tincture U.S.P. 2%

Purpose

First aid antiseptic

Use

First aid to help prevent skin infection in

• minor cuts
• scrapes
• burns

Warnings

For external use only

Ask a doctor before use

if you have deep or puncture wounds, animal bites or serious burns

When using this product

• 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

condition persists or gets worse

Keep out of reach of children.

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

Directions

• 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

none

Other information

Product will stain skin and clothing

SPL UNCLASSIFIED SECTION

Distributed by SUPERVALU INC., Eden Prairie, MN 55344 USA

Contact us at 1-877-932-7948 or www.supervalu-ourownbrands.com

088.00/088AA

principal display panel

EQUALINE

iodine tincture USP

first aid antiseptic

for external use only

CAUTION POISON

1 OZ (30 mL)

INGREDIENTS AND APPEARANCE

IODINE 
iodine liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 41163-088
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4)	IODINE	20 mg  in 1 mL
SODIUM IODIDE (UNII: F5WR8N145C) (IODIDE ION - UNII:09G4I6V86Q)	IODIDE ION	20.4 mg  in 1 mL
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	470 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 41163-088-10	30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/04/2005

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	02/04/2005

Labeler - Supervalu Inc. (006961411)

Registrant - Vi-Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Humco Holding Group, Inc		825672884	manufacture(41163-088)