IODINE TINCTURE WHITE- iodine tincture solution/ drops

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

Iodine 2%

Available from:

Dannso Corp./d.b.a. Essential Products

Administration route:

TOPICAL

Prescription type:

OTC DRUG

Therapeutic indications:

First aid antiseptic First aid to help prevent sking infection in - minor cuts - scrapes - burns If condition persists or gets worse

Authorization status:

OTC monograph not final

Summary of Product characteristics

IODINE TINCTURE WHITE- IODINE TINCTURE SOLUTION/ DROPS
DANNSO CORP./D.B.A. ESSENTIAL PRODUCTS
----------
IODO BLANCO
ACTIVE INGREDIENTS
Iodine 2%
PURPOSE
First aid antiseptic
USE
First aid to help prevent sking infection in
minor cuts
scrapes
burns
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
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)
Dannso Corp./d.b.a. Essential Products
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 Drug
M