MEDLINE NASAL ANTISEPTIC SWABS- povidone iodine swabstick solution 
Medline Industries, LP

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497 Medline Nasal Antiseptic Swabs

Active ingredient

Povidone-iodine USP 10%

Purpose

Antiseptic

Uses

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:

Figure

  • Use a tissue to clean the inside of both nostrils, including the inside tip of nostril. Discard.

Figure

  • Insert swab comfortably into one nostril and rotate for 30 seconds, covering all surfaces. Discard swabstick.

Figure

  • Using a 2nd swab, repeat step 2 with the other nostril.

Figure

  • Repeat the application in both nostrils, using the 3rd and 4th swabs.

Figure

  • Do not blow nose. If solution drips, gently wipe with a tissue.

Other information

Inactive ingredients

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

Manufacturing Information

Manufactured by:

Medline Industries, LP

Three Lakes Drive, Northfield IL 60093 USA

Made in USA

1-800-MEDLINE (633-5463)

REF: MDS1982

V1 RG22APL

Package Label

Label Front

Label Back

MEDLINE NASAL ANTISEPTIC SWABS 
povidone iodine swabstick solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53329-497
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE10 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:53329-497-422 in 1 BOX01/15/2018
1NDC:53329-497-2610 mL in 1 PACKET; Type 0: Not a Combination Product
2NDC:53329-497-66250 in 1 CASE01/15/2018
2NDC:53329-497-2610 mL in 1 PACKET; Type 0: Not a Combination Product
3NDC:53329-497-2610 mL in 1 PACKET; Type 0: Not a Combination Product01/15/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)01/15/2018
Labeler - Medline Industries, LP (025460908)
Registrant - Medline Industries, LP (025460908)

Revised: 11/2023
Document Id: 0b64e78c-78e9-96c0-e063-6394a90a939b
Set id: 6282442b-353e-bf51-e053-2a91aa0a266a
Version: 9
Effective Time: 20231130
 
Medline Industries, LP