HALODINE NASAL ANTISEPTIC- povidone-iodine solution 
Halodine LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Halodine Nasal Antiseptic

Drug Facts

Active Ingredient

Povidone-Iodine USP, 1.25%

(0.125% Available Iodine)

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
  • Over large areas of the body

Ask a doctor before use if injuries are

  • Deep or puncture wounds
  • Serious burns

Stop use and ask a doctor if

irritation and redness develop or if condition persists for more than 72 hours.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

For nasal application

  1. Gently blow nose to clear both nostrils. Discard tissue.
  2. Open single ampoule by tearing off the narrow end along line. To avoid spill while opening, only hold flat foil around raised body of ampoule and maintain ampoule with narrow end pointing up.
  3. Place narrow end of ampoule at right nostril and gently pinch left nostril. Lift chin and tilt head back; squeeze all liquid from ampoule while inhaling through right nostril. Discard ampoule.
  4. Open second ampoule by tearing off the narrow end along line. Avoid spill.
  5. Place narrow end of ampoule at left nostril and gently pinch right nostril. Lift chin and tilt head back; squeeze all liquid from ampoule while inhaling through left nostril. Discard ampoule.

Note: Do not blow nose. If solution drips, wipe with tissue.

Other Information

Inactive Ingredients

hydroxyethylcellulose, purified water

Questions or comments?

contact@halodine.com

Principal Display Panel

Halodine 101.02

HALODINE NASAL ANTISEPTIC 
povidone-iodine solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78371-101
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE1.25 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:78371-101-02100 in 1 CARTON06/15/2020
11.5 mL in 1 AMPULE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E06/15/2020
Labeler - Halodine LLC (117526113)

Revised: 8/2020
Document Id: acd96f6a-6c21-3166-e053-2a95a90a8134
Set id: acd96f6a-6c20-3166-e053-2a95a90a8134
Version: 1
Effective Time: 20200814
 
Halodine LLC