POVIDONE IODINE 10%- povidone iodine liquid

Drug Labeling and Warnings

Drug Details [pdf]

Drug Facts Active ingredient

Povidone-Iodine 10%
(Equivalent to 1% titratable iodine)

Purpose

First Aid Antiseptic

Uses

First aid to help prevent infection in minor cuts, scrapes and burns

Warnings

For external use only.

Do not use

■ in the eyes
■ over large areas of the body
■ for longer than 1 week unless directed by a doctor
■ on individuals who are allergic or sensitive to iodine

Ask a doctor before use if you have

■ deep or puncture wounds
■ animal bites
■ serious burns

Stop use and ask a doctor if

■ the condition persists or gets worse
■ irritation or redness develops or persists

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 on the area 1 to 3 times daily
■ may be covered with sterile bandage
■ if bandaged let dry first

Other information

■ store at room temperature, 20-25°C (68-77° F)

Inactive ingredients

Citric acid, disodium phosphate, glycerin, nonoxynol-9, sodium hydroxide and purified water

Questions or comments?

(855)-280-1079

Principal Display Panel

NDC: 85786-702-08

DR. SIMI

Povidone Iodine
10% Topical Solution

FIRST AID ANTISEPTIC

Helps prevent infection in minor
cuts scrapes burns

8 fl oz (237 mL)

Distributed by:
FARMACIAS DE SIMILARES TX LLC.
800 Brazos St Ste 260, Austin, TX, 78701, USA
customerservice@drsimi.com
www.drsimi.com

†Compare to Active Ingredient in Betadine®

†This product is not manufactured or distributed by Atlantis Consumer Healthcare Inc., owner of the registered trademark Betadine®.

Immediare container labeling

INGREDIENTS AND APPEARANCE

POVIDONE IODINE 10% 
povidone iodine liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85786-702
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4)	IODINE	100 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE (UNII: 70WT22SF4B)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
NONOXYNOL-9 (UNII: 48Q180SH9T)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85786-702-08	237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/01/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	04/01/2026

Labeler - Farmacias De Similares TX LLC (119489934)

Establishment
Name	Address	ID/FEI	Business Operations
Pharma Nobis, LLC		118564114	manufacture(85786-702) , label(85786-702) , pack(85786-702) , analysis(85786-702)