HUMCO STRONG IODINE TINCTURE- iodine tincture liquid

Humco Strong Iodine Tincture by

Drug Labeling and Warnings

Humco Strong Iodine Tincture by is a Otc medication manufactured, distributed, or labeled by Humo Holding Group, Inc., Humco Holding Group, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

Iodine 7%

Potassium Iodide 5%

alcohl 85%

Purpose

Antiseptic

Uses

To prevent infection in mior cuts, scrapes, and burns.

Warnings

For external use only

Ask a doctor if you have:

deep or puncture wounds

animal bites

serious burns.

Stop use and consult a doctor if:

The condition persists or gets worse, or if using for longer than once a week.

When using this product:

Do not use in the eyes. If contact occurs, flush with large amounts of water 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

Clean affacted area

Apply a small amount on the area 1 to 3 times daily.

May be covered with sterile bandage.

If bandaged, let it dry first.

Inactive Ingredient

Purified water

Principal Display Panel

Label

INGREDIENTS AND APPEARANCE

HUMCO STRONG IODINE TINCTURE 
iodine tincture liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0395-1219
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4)	IODINE	70 mg  in 1 mL
POTASSIUM IODIDE (UNII: 1C4QK22F9J) (IODIDE ION - UNII:09G4I6V86Q)	IODIDE ION	50 mg  in 1 mL
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	850 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: 0395-1219-16	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/09/2017	07/31/2021
2	NDC: 0395-1219-91	30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/09/2017	07/31/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/25/1998	07/31/2021

Labeler - Humo Holding Group, Inc. (825672884)

Registrant - Humo Holding Group, Inc. (825672884)

Establishment
Name	Address	ID/FEI	Business Operations
Humco Holding Group, Inc.		825672884	manufacture(0395-1219) , label(0395-1219) , analysis(0395-1219) , pack(0395-1219)