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

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Humco 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

Old Label



Principal Display Panel NDC 0395-1213-16 IODINE TINCTURE 2% MILD USP ALCOHOL 47% 16 FL OZ(30mL)

New Label

New Label

IODINE TINCTURE MILD 
iodine and sodium iodide and alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0395-1213
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:0395-1213-16473 mL in 1 BOTTLE; Type 0: Not a Combination Product11/14/2017
2NDC:0395-1213-9130 mL in 1 BOTTLE; Type 0: Not a Combination Product11/14/2017
3NDC:0395-1213-55208000 mL in 1 DRUM; Type 0: Not a Combination Product02/21/201412/19/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00301/01/1979
Labeler - Humco Holding Group, Inc. (825672884)
Registrant - Pharma Nobis, LLC (118564114)
Establishment
NameAddressID/FEIBusiness Operations
Pharma Nobis, LLC118564114manufacture(0395-1213) , analysis(0395-1213) , pack(0395-1213) , label(0395-1213)

Revised: 12/2023
Document Id: 0c9325b5-94b7-f74e-e063-6394a90ab2ee
Set id: 41c0927e-df40-4f83-8fd4-284ec0c02b60
Version: 7
Effective Time: 20231215
 
Humco Holding Group, Inc.