PREMIER VALUE IODINE TINCTURE MILD- iodine and sodium iodide and alcohol liquid 
Chain Drug Consortium

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 Ticture

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

Label

PV Iodine

PREMIER VALUE IODINE TINCTURE MILD 
iodine and sodium iodide and alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68016-121
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:68016-121-9130 mL in 1 BOTTLE; Type 0: Not a Combination Product10/27/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A10/27/2017
Labeler - Chain Drug Consortium (101668460)
Registrant - Humco Holding Group, Inc (825672884)
Establishment
NameAddressID/FEIBusiness Operations
Humco Holding Group, Inc.825672884manufacture(68016-121) , analysis(68016-121) , pack(68016-121) , label(68016-121)

Revised: 12/2020
Document Id: b6d946bc-d0c0-3599-e053-2995a90a6302
Set id: 5c89937d-2465-902e-e053-2a91aa0accf4
Version: 2
Effective Time: 20201219
 
Chain Drug Consortium