DE LA CRUZ DECOLORIZED IODINE- ethyl alcohol liquid

De La Cruz Decolorized Iodine by

Drug Labeling and Warnings

De La Cruz Decolorized Iodine by is a Otc medication manufactured, distributed, or labeled by DLC Laboratories, Inc., Pharma Nobis, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

IODIDES TINCTURE- ethyl alcohol liquid Humco Holding Group, Inc.

Private Label Iodides Tincture

Drug Facts

Active Ingredients

Alcohol 45% denatured with ammonia, Ammonium and Potassium Iodides.

Purpose

Antiseptic

Uses

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.

Stop use and ask a doctor if:

The condition persists or gets worse, or if using this product for longer than 1 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 the reach of children.

      In case of accidental ingestion give milk, then give a starch solution made by mixing two tablespoonsful of cornstarch or flour into a pint of water. Contact a Poison Control Center immediately.

Directions

Clean the affected area. Apply a small amount to the affected area 1 to 3 times daily. May be covered with a sterile bandage. Allow affected area to dry completely, before applying sterile bandage.

Inactive Ingredient:

Purified Water

Other Information:

Will stain skin and clothing

De La Cruz Label

Principal display Panel

De La Cruz
Decolorized Iodine
Yodo Blanco
Alcohol 48%
1 FL OZ
(30 mL)

INGREDIENTS AND APPEARANCE

DE LA CRUZ DECOLORIZED IODINE 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 24286-1529
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.45 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
AMMONIA (UNII: 5138Q19F1X)
IODINE (UNII: 9679TC07X4)
POTASSIUM IODIDE (UNII: 1C4QK22F9J)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 24286-1529-8	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/06/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333A	03/25/1998

Labeler - DLC Laboratories, Inc. (093351930)

Registrant - Humco Holding Group, Inc (825672884)