10% POVIDONE IODINE NASAL SWAB- povidone iodine nasal swab solution

Active ingredient

Povidone-iodine USP 10%
Purpose

Antiseptic
Uses
- antiseptic skin preparation
- helps reduce bacteria that can potentially cause skin infections
Warnings
For external use only
Do not use
- if allergic to iodine
- in the eyes
- on children less than 3 years old
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 persists or increases
- infection occurs
Keep out of reach of children.

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

Avoid excessive heat.Store at room temperature.

Directions

NASAL APPLICATION:

	Use a tissue to clean the inside of both nostrils, including the inside tip of nostril. Discard.
	Insert swab comfortably into one nostril and rotate for 30 seconds, covering all surfaces. Discard swabstick.
	Using a 2nd swab, repeat step 2 with the other nostril.
	Repeat the application in both nostrils, using the 3rd and 4th swabs.
	Do not blow nose. If solution drips, gently wipe with a tissue.

Other information
- 1% titratable iodine
- not made with natural rubber latex
- for hospital or professional use only
Inactive ingredients

disodium phosphate, glycerin, hydroxyethylcellulose, nonoxynol-10, simethicone, water
Package Label

INGREDIENTS AND APPEARANCE

10% POVIDONE IODINE NASAL SWAB
povidone iodine nasal swab solution

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

Ingredient Name	Strength
Inactive Ingredients
DIMETHICONE (UNII: 92RU3N3Y1O)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)
HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) (UNII: S38J6RZN16)
NONOXYNOL-10 (UNII: K7O76887AP)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC: 83062-497-26	10 mL in 1 PACKET; Type 0: Not a Combination Product	10/15/2023

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	10/15/2023

Labeler - IIMED MEDICAL MEXICANA S DE RL DE CV (812894376)

Registrant - Medline Industries, LP (025460908)

Name	Address	ID/FEI	Business Operations
Establishment
IIMED MEDICAL MEXICANA S DE RL DE CV		812894376	relabel(83062-497) , repack(83062-497)

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