TRIADINE PREP- povidone-iodine solution

Triadine Prep by

Drug Labeling and Warnings

Triadine Prep by is a Otc medication manufactured, distributed, or labeled by Triad Group. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Povidone Iodine,10% w/v (equivalent to 1% titratable iodine)

PURPOSE

Antiseptic

USES

• Health-care antiseptic for preparation of the skin prior to surgery
• First id antiseptic to help prevent the risk of infection in minor cuts, scrapes and burns.
  

WARNINGS

For external use only.

Do not use

• in the eyes
• on individuals who are allergic or sensitive to iodine
• as a first aid antiseptic for longer than 1 week

Ask a doctor in case of

• deep or puncture wounds
• animal bites
• serious burns
  

Stop use and ask a doctor

• if irritation and redness develop
  

Keep out of reach of children

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

DIRECTIONS

For preparation of the skin prior to surgery:

• clean the area
• apply to the operative site prior to surgery

As a first aid antiseptic

• clean the affected area
• apply a small amount of this product to the area 1-3 times daily
• may be covered with a sterile bandage
• if bandaged, let dry first
  

SPL UNCLASSIFIED SECTION

OTHER INFORMATION

store at 15° - 30° C (59° - 86° F)

INACTIVE INGREDIENTS

citric acid, glycerin, nonoxynol-8, sodium hydroxide, water

QUESTIONS

LABEL INFORMATION

Cat. No. 10-8204
NDC: 50730-8204-4

TRIADINE™

POVIDONE-IODINE, USP
PREP SOLUTION
10% Topical Solution

ANTISEPTIC / GERMICIDE

• ANTISEPTIC for preparation of the skin prior to surgery. Helps reduce bacteria that potentially can cause skin infection.
• FIRST AID ANTISEPTIC to help prevent the risk of infection in minor cuts, scrapes and burns.
• For Hospital and Professional Use.
  

For External Use Only!

4 Fluid Ounces (118 ml)

www.triad-group.net

TRIAD GROUP, INC.
700 West North Shore Drive
Hartland, WI 53029 MADE IN USA

INGREDIENTS AND APPEARANCE

TRIADINE PREP 
povidone-iodine solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50730-8204
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
povidone-iodine (UNII: 85H0HZU99M) (povidone-iodine - UNII:85H0HZU99M)	povidone-iodine	.10 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
citric acid monohydrate (UNII: 2968PHW8QP)
glycerin (UNII: PDC6A3C0OX)
sodium hydroxide (UNII: 55X04QC32I)
water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50730-8204-3	118 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333	06/21/1985

Labeler - Triad Group (050259597)

Establishment
Name	Address	ID/FEI	Business Operations
Triad Group		050259597	manufacture