IODINE TINCTURE WHITE- iodine tincture solution/ drops

Iodine Tincture White by

Drug Labeling and Warnings

Iodine Tincture White by is a Otc medication manufactured, distributed, or labeled by Dannso Corp./d.b.a. Essential Products, World Perfume, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Iodine 2%

Purpose

First aid antiseptic

Use

First aid to help prevent sking infection in

• minor cuts
• scrapes
• burns

WARNINGS

Warnings

For external use only. Avoid contact with eyes or with mucous membrane. Keep out of the reach of children. Children under 2 years please consult a physician. Do not apply on irritated skin, in or near eyes or mocuos memebranes, on wounds or damamged skin, or if it causes allergic reaction. In case of accidental ingestion, seek professional assistance or contact Poison Control Center immedialately.

Inactive Ingredient

Ammonium, Deionized Water, Isopropyl Alcohol, Sodium Iodine.

Stop use and ask a doctor

If condition persists or gets worse

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away

Directions

• Clean the affected area and dry thorougkyapply.
• Apply a thin layer 1 to 3 times daily
• May be covered with a sterile bandage

Questions or Comments?

Distributed by

Essential Products Miami FL 33126

www.essentialproductsuse.com

Made in U.S.A.

Principal display panel

IODO BLANCO

INGREDIENTS AND APPEARANCE

IODINE TINCTURE WHITE 
iodine tincture solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70242-109
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

Inactive Ingredients
Ingredient Name	Strength
AMMONIUM SALICYLATE (UNII: 0T3Q181657)
Isopropyl Alcohol (UNII: ND2M416302)
Sodium Iodide (UNII: F5WR8N145C)
water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70242-109-01	30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/08/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/08/2015

Labeler - Dannso Corp./d.b.a. Essential Products (059741071)

Registrant - Dannso Corp./d.b.a. Essential Products (059741071)

Establishment
Name	Address	ID/FEI	Business Operations
Dannso Corp./d.b.a. Essential Products		059741071	LABEL(70242-109)

Establishment
Name	Address	ID/FEI	Business Operations
World Perfume, Inc		101312044	MANUFACTURE(70242-109)