POVIDONE IODINE PREP PAD- povidone-iodine solution

Povidone Iodine Prep Pad by

Drug Labeling and Warnings

Povidone Iodine Prep Pad by is a Otc medication manufactured, distributed, or labeled by H and P Industries, Inc. dba 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

• First Aid Antiseptic to help prevent infection in minor cuts, scrapes and burns
• Health Care Antiseptic for preparation of the skin prior to surgery

WARNINGS

For external use only.

Do not use

• in the eyes
• apply over large areas of the body
• use on individuals who are allergic or sensitive to iodine
• use as a first aid antiseptic for longer than 1 week unless directed by a doctor

Ask a doctor in case of

• deep or puncture wounds
• animal bites
• serious burns
  

Stop use and ask a doctor

• if condition persists for more than 72 hours
• 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

• clean the affected area
• apply a small amount of this product to the area 1-3 times daily and discard
  
• may be covered with a sterile bandage when dry
  

SPL UNCLASSIFIED SECTION

OTHER INFORMATION

Store at room temperature 15° - 30° C (59° - 86° F)

INACTIVE INGREDIENTS

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

QUESTIONS

PACKAGE INFORMATION

Triad

Cat. No. 10-3201
NDC: 50730-3201-1

Povidone Iodine
Prep Pads

Antiseptic / Germicide

• Helps prevent the risk of infection in minor cuts, scrapes and burns
• Health-care antiseptic for preparation of the skin prior to surgery
• For Professional and Hospital Use Only
• 10% Povidone Iodine, USP
  

Latex Free

100 Pads

Triad Group, Inc.
700 West North Shore Drive
Hartland, WI 53029
www.triad-group.net
1-800-288-1288

MADE IN USA

INGREDIENTS AND APPEARANCE

POVIDONE IODINE PREP PAD 
povidone-iodine solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50730-3201
Route of Administration	TOPICAL, EPIDURAL, PERCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
povidone-iodine (UNII: 85H0HZU99M) (povidone-iodine - UNII:85H0HZU99M)	povidone-iodine	.10 g

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: 50730-3201-1	100 in 1 CARTON
1		1 in 1 POUCH

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

Labeler - H and P Industries, Inc. dba Triad Group (050259597)

Registrant - H and P Industries, Inc. dba Triad Group (050259597)

Establishment
Name	Address	ID/FEI	Business Operations
H and P Industries, Inc. dba Triad Group		050259597	manufacture