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

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.

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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 acidental ingestion give milk, then give a starch solution made by mixing two tablespoonfools of cornstarch or flour to a pint of water. contact a poison Control Center immediately.

Directions

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

Inactive Ingredient:

Purified Water

Other Information:

Will stain skin and clothing

De La Cruz Label

DLC

Good Neighbor Label

GNP

Leader Label

Leader

Quality Choice Label

Sunmark Label

DDM Label

DDM

Rite Aid Label

CVS Label

CVC

Top Care Label

Vida Mia Label

Health Mart Label

IODIDES TINCTURE
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0395-9117
Route of Administration	TOPICAL

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

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

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:0395-9117-92	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/30/2017
2	NDC:0395-9117-91	30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/30/2017

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

Labeler - Humco Holding Group, Inc. (825672884)

Registrant - Humco Holding Group, Inc. (825672884)

Name	Address	ID/FEI	Business Operations
Establishment
Humco Holding Group, Inc.		825672884	manufacture(0395-9117) , analysis(0395-9117) , pack(0395-9117) , label(0395-9117)

Revised: 12/2017

Document Id: 6062fd98-7662-f4b5-e053-2a91aa0acbc3

Set id: 6062fd98-7661-f4b5-e053-2a91aa0acbc3

Version: 1

Effective Time: 20171215

Humco Holding Group, Inc.