Iodine Tincture

Iodine Tincture

Drug Labeling and Warnings

Drug Details

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IODINE TINCTURE- iodine tincture solution/ drops 
Kroger Co

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Iodine Tincture

Active ingredient

Iodine tincture USP 100% (2% iodine)

Purpose

First aid antiseptic

Use

First aid to help prevent sking 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

Questions or Comments?

1-800-632-6900

DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO 45202

www.kroger.com

Principal display panel

FIRST AID ANTISEPTIC

KRGER

IODINE TINCTURE USP

FOR EXTERNAL USE ONLY

CAUTION POISON

1 FL OZ (30 mL)

image description

088.000/088AA

IODINE TINCTURE 
iodine tincture solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 30142-088
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE20 mg  in 1 mL
SODIUM IODIDE (UNII: F5WR8N145C) (IODIDE ION - UNII:09G4I6V86Q) IODIDE ION20.4 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
water (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 30142-088-1030 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/21/2001
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A06/21/2001
Labeler - Kroger Co (006999528)
Registrant - Vi-Jon (790752542)
Establishment
NameAddressID/FEIBusiness Operations
Humco Holding Group, Inc825672884manufacture(30142-088)

Revised: 12/2018
 
Kroger Co


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