QUALITY CHOICE IODINE TINCTURE MILD- iodine and sodium iodide and alcohol liquid 
Chain Drug Market Association

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Quality Choice Iodine Ticture

Drug Facts

Active ingredient

Iodine Tincture, USP 2%, Mild

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

none

Principal Display Panel

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

QUALITY CHOICE IODINE TINCTURE MILD 
iodine and sodium iodide and alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63868-330
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:63868-330-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product12/12/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00301/01/1979
Labeler - Chain Drug Market Association (011920774)
Registrant - Pharma Nobis, LLC (118564114)
Establishment
NameAddressID/FEIBusiness Operations
Pharma Nobis, LLC118564114manufacture(63868-330) , analysis(63868-330) , pack(63868-330) , label(63868-330)

Revised: 12/2023
Document Id: 0cf49a57-812c-2985-e063-6294a90aa887
Set id: 55c970ed-13a9-4ea2-a8cb-aaf14d3a214d
Version: 5
Effective Time: 20231220
 
Chain Drug Market Association