IODINE TINCTURE MILD- iodine and sodium iodide and alcohol liquid 
Humco Holding Group, Inc.

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.

----------

Private Label Iodine Ticture Mild, USP

Drug Facts

Active ingredient

Iodine 2%

Purpose

First Aid Antiseptic

Active ingredient

Sodium Iodide 2.4%

Purpose

First Aid Antiseptic

Active ingredient

Alcohol 47%

Purpose

First Aid Antiseptic

Indications

First aid to help prevent infection in minor cuts, scrapes and burns

Warnings      

For external use only.

Ask a doctor before use if you have

  • deep or puncture wounds
  • animal bites
  • serious burns
  • Flammable: Keep away from sparks heat and flame

Stop use and consult doctor if

  • the condition persists or gets worse, or if using for longer than one week

When using this product

  • do not use in the eyes. If contact occurs, flush with large amounts of water while lifting upper and lower lids
  • do not apply over large areas of the body

Keep out of reach of children.

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

Other information

Inactive ingredient

Purified Water

Good Neighbor Label

GNP

Leader Label

LDRMild.jpgLeader

Quality Choice Label

QC

Sunmark Label

SMMild.jpgSunmark

Premier Value Label

PVMild.jpgPV

DDM Label

DDM

De La Cruz Label

DLCMild.jpgDLC

CVS Label

CVS Iodine 1CVSMild.jpgCVS

Harris Teeter Label

HT

Kroger Label

KrogerMild.jpgKroger

Safeway Label

Safeway

Vida Mia Label

VM

Swan Label

SwanMild.jpgSwan

Good Sense Label

GoodSenseMild.jpgGood Sense

Walgreen Label

Walgreens Iodine 1WallgreensMild.jpgWalgreen

Health Mart Label

HM

Equaline Label

EqualineMild.jpgEqualine

IODINE TINCTURE MILD 
iodine and sodium iodide and alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0395-9118
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
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL470 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0395-9118-9130 mL in 1 BOTTLE; Type 0: Not a Combination Product11/14/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/01/1979
Labeler - Humco Holding Group, Inc. (825672884)
Registrant - Humco Holding Group, Inc. (825672884)
Establishment
NameAddressID/FEIBusiness Operations
Humco Holding Group, Inc.825672884manufacture(0395-9118) , analysis(0395-9118) , pack(0395-9118) , label(0395-9118)

Revised: 12/2021
Document Id: d3d2c393-cbb3-d293-e053-2a95a90ad250
Set id: 6063529b-f3d0-1c8b-e053-2a91aa0a9395
Version: 4
Effective Time: 20211223
 
Humco Holding Group, Inc.