STRONG IODINE TINCTURE- iodine tincture liquid 
Humo 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.

----------

Humco Strong Iodine Tincture

Drug Facts

Active Ingredient

Alcohol 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

Iodine 7%, Potassium Iodide 5%, Purified water

Label

label

STRONG IODINE TINCTURE 
iodine tincture liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0395-1220
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL850 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
IODINE (UNII: 9679TC07X4)  
POTASSIUM IODIDE (UNII: 1C4QK22F9J)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0395-1220-16473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/09/2017
2NDC:0395-1220-9130 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/09/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A11/09/2017
Labeler - Humo Holding Group, Inc. (825672884)
Registrant - Humo Holding Group, Inc. (825672884)
Establishment
NameAddressID/FEIBusiness Operations
Humco Holding Group, Inc.825672884manufacture(0395-1220) , label(0395-1220) , analysis(0395-1220) , pack(0395-1220)

Revised: 11/2017
Document Id: 5d9340bf-91fc-7f15-e053-2a91aa0a1195
Set id: 5d93562d-f6af-c699-e053-2a91aa0aec3b
Version: 1
Effective Time: 20171109
 
Humo Holding Group, Inc.