POVIDONE-LODINE PREP PAD patch

Povidone-lodine prep pad by

Drug Labeling and Warnings

Povidone-lodine prep pad by is a Otc medication manufactured, distributed, or labeled by SHENZHEN BENLIJU BIO-TECH CO.,LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Available Iodine

PURPOSE

disinfect

INDICATIONS & USAGE

For preparation of the skin prior to an injection and to decrease germs in minor cuts and scrapes.

WARNINGS

*For extemal use only.
*Flammable. keep away from fire or flame.

DO NOT USE

Do not use " with electrocautery procedures " in the eyes. lf contact occurs, flush eyes with water.

WHEN USING

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

STOP USE

*Stop use if irritation and redness develop. If condition persists consult your health care practioner.

*Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

For preparation of the skin prior to an injection and to decrease germs in minor cuts and scrapes.One piece at a time.

STORAGE AND HANDLING

Store at room temperature.

INACTIVE INGREDIENT

water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

POVIDONE-LODINE PREP PAD 
povidone-lodine prep pad patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84449-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4)	IODINE	10 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84449-002-01	1 g in 1 PATCH; Type 0: Not a Combination Product	08/20/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	08/20/2024

Labeler - SHENZHEN BENLIJU BIO-TECH CO.,LTD (551073413)

Registrant - SHENZHEN BENLIJU BIO-TECH CO.,LTD (551073413)

Establishment
Name	Address	ID/FEI	Business Operations
SHENZHEN BENLIJU BIO-TECH CO.,LTD		551073413	manufacture(84449-002)