DE LA CRUZ TINCTURE OF IODINE- iodine and sodium iodide and alcohol liquid 
DLC Laboratories, Inc.

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De La Cruz Tincture of Iodine

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

dlciod.jpglabel

DE LA CRUZ TINCTURE OF IODINE 
iodine and sodium iodide and alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24286-1528
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:24286-1528-730 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 DrugM00301/01/1979
Labeler - DLC Laboratories, Inc. (093351930)
Registrant - Pharma Nobis, LLC (118564114)
Establishment
NameAddressID/FEIBusiness Operations
Pharma Nobis, LLC118564114manufacture(24286-1528) , analysis(24286-1528) , pack(24286-1528) , label(24286-1528)

Revised: 12/2023
Document Id: 0c940d4f-cca2-7175-e063-6394a90af568
Set id: 5d8f60a9-6d1c-0b0f-e053-2991aa0a8a9b
Version: 5
Effective Time: 20231215
 
DLC Laboratories, Inc.