LIGHTS POVINDONE IODINE SCRUB- povidone-iodine solution

Lights Povindone Iodine Scrub by

Drug Labeling and Warnings

Lights Povindone Iodine Scrub by is a Otc medication manufactured, distributed, or labeled by Lights Medical Manufacture Co., Ltd., Lights Medical Manufacture Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient: Povidone-Iodine USP (7.5%)

PURPOSE

Purpose: Antiseptic

INDICATIONS & USAGE

Use:

Antiseptic skin preparation

WARNINGS

Warnings:

Do not use if allergic to iodine

For external use only

Do not use in eyes

Avoid pooling beneath patient. Prolonged exposure to wet solution may cause skiin irritation.

ASK DOCTOR

Ask a doctor before use if injuries are

deep or puncture wounds

Serious burns

Stop use and ask a doctor if 

Redness, irritation, swelling or pain persisits or increases

Infection occurs

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. In case of a accidental ingestion,, seek professional assistance or consult a poison control center immediately

DOSAGE & ADMINISTRATION

Directions:

Apply locally as needed.

OTHER SAFETY INFORMATION

Other information

• Store at room temperature
• 0.75% available iodine
• Latax free
• For hospital or professional use only

INACTIVE INGREDIENT

Inactive Ingredient

Citric acid, purified water, Disodium hydrogen phosphate

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LIGHTS POVINDONE IODINE SCRUB 
povidone-iodine solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 61333-205
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4)	IODINE	0.75 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM PHOSPHATE DIBASIC DIHYDRATE (UNII: 94255I6E2T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 61333-205-01	118 g in 1 BOTTLE; Type 0: Not a Combination Product	07/18/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333C	07/18/2019

Labeler - Lights Medical Manufacture Co., Ltd. (529128649)

Registrant - Lights Medical Manufacture Co., Ltd. (529128649)

Establishment
Name	Address	ID/FEI	Business Operations
Lights Medical Manufacture Co., Ltd.		529128649	manufacture(61333-205)