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De La Cruz Tincture of Iodine

Dosage form: liquid
Ingredients: IODINE 20mg in 1mL, SODIUM IODIDE 20.4mg in 1mL, ALCOHOL 470mg in 1mL
Labeler: DLC Laboratories, Inc.
NDC Code: 24286-1528

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.

DE LA CRUZ® TINCTURE OF IODINE

Drug Facts

Active ingredients

Iodine 2%, Sodium Iodide 2.4%

Purpose

First aid antiseptic

Uses

First aid antiseptic to help prevent infection in minor:

  • cuts
  • scrapes
  • burns

Warnings

For external use only

Flammable. Keep away from sparks, heat and fire.

Consult a doctor before use if you have
  • deep or puncture wounds
  • animal bites
  • serious burns

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

Stop use and consult a doctor if
  • the condition persists or gets worse. Do not use this product longer than 1 week unless directed by a doctor.

Keep out of reach of children.

If swallowed, give milk then give a starch solution made by mixing 2 tablespoons of corn starch or flour to a pint of water. Contact a Poison Control Center immediately.

Directions
  • clean the affected area
  • apply a small amount of this product to the area 1 to 3 times daily
  • may be covered with a sterile bandage. If bandaged, let dry first.

Other information
  • will stain skin and clothing
  • store at room temperature

Inactive ingredients

alcohol, purified water

Questions

1-800-858-3889

Distributed by:
De La Cruz Products
A Division of DLC Laboratories, Inc.
Paramount, CA 90723 USA

PRINCIPAL DISPLAY PANEL - 30 mL Bottle Label

De La Cruz®

Tincture
of Iodine

USP 2% • Alcohol 47%

First Aid Antiseptic

TRUSTED
QUALITY

For External Use Only

POISON / DANGER

1 FL OZ
(30 mL)

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 AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
IODINE (IODINE) IODINE20 mg  in 1 mL
SODIUM IODIDE (IODIDE ION) IODIDE ION20.4 mg  in 1 mL
ALCOHOL (ALCOHOL) ALCOHOL470 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
Packaging
#Item CodePackage Description
1NDC:24286-1528-730 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/01/1979
Labeler - DLC Laboratories, Inc. (093351930)
Registrant - Humco Holding Group, Inc (825672884)

 
DLC Laboratories, Inc.

Medically reviewed on Jul 17, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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