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

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Humco 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

Pther Information:

Will stain skin and clothing

New label

Decolorized.jpg

HUMCO IODIDES TINCTURE 
ethyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0395-1207
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.45 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
AMMONIA (UNII: 5138Q19F1X)  
IODINE (UNII: 9679TC07X4)  
POTASSIUM IODIDE (UNII: 1C4QK22F9J)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0395-1207-9259 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/30/2017
2NDC:0395-1207-16473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/30/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00303/25/1998
Labeler - Humco Holding Group, Inc. (825672884)
Registrant - Pharma Nobis, LLC (118564114)
Establishment
NameAddressID/FEIBusiness Operations
Pharma Nobis, LLC118564114manufacture(0395-1207) , analysis(0395-1207) , pack(0395-1207) , label(0395-1207)

Revised: 12/2023
Document Id: 0c931a56-b7e0-c70e-e063-6394a90a2c4a
Set id: d230e3a2-1cde-44a9-82c3-3dc5474b3a72
Version: 9
Effective Time: 20231215
 
Humco Holding Group, Inc.