GNP IDOINDE TINCTURE 2% MILD- iodine and sodium iodide and alcohol liquid

GNP Idoinde Tincture 2% Mild by

Drug Labeling and Warnings

GNP Idoinde Tincture 2% Mild by is a Otc medication manufactured, distributed, or labeled by Amerisource Bergen, Pharma Nobis, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug facts

Active Ingredients

Iodine 2%

Sodium iodide 2.4%

Alcohol 47%

Purpose

Antiseptic

Uses:

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

condition persists or gets worse, or if using this product for longer than 1 week.

When using this product.

Do not use in eyes. If contact occurs, flush with large amounts of water while lifting upper and lower eyelids.

Do not apply over large areas of the body.

Keep out of reach ofchildren

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

Directions:

Clean the affected area. Apply a small amount to the affeted area 1 to 3 times daily. May be covered with sterile bandage. If bandaged, let dry first.

Inactive ingredient:

Purified Water.

Other information:

Will stain skin and clothing

Dist. by: AmerisourceBergen

1300 Morris Dr., Chesterbrook, PA 19087

Questions or Comments?

1-800-662-3435     www.goodneighborpharmacy.com

Principal Display Panel

Good Neighbor Pharmacy   NDC: 24385-0213-10

Iodine Tincture USP 2% Mild

Antiseptic First Aid

First Aid Antiseptic

Alcohol 47%

FLAMMABLE: Keep away from sparks, heal & flame.

1 FL OZ (30 mL)

INGREDIENTS AND APPEARANCE

GNP IDOINDE TINCTURE 2% MILD 
iodine and sodium iodide and alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 24385-213
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4)	IODINE	20 mg  in 1 mL
SODIUM IODIDE (UNII: F5WR8N145C) (IODIDE ION - UNII:09G4I6V86Q)	IODIDE ION	20.4 mg  in 1 mL
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	470 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 24385-213-10	30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/16/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/01/2008

Labeler - Amerisource Bergen (007914906)

Registrant - Humco Holding Group, Inc. (825672884)

Establishment
Name	Address	ID/FEI	Business Operations
Humco Holding Group, inc.		825672884	manufacture(24385-213) , analysis(24385-213) , pack(24385-213) , label(24385-213)