CLOROX HEALTHCARE NASAL ANTISEPTIC SWABS- povidone iodine swabstick solution 
Aplicare Products, 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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0972 Clorox Healthcare Nasal Antiseptic Swabs

Povidone-iodine USP10%

Antiseptic

  • antiseptic skin preparation
  • helps reduce bacteria that can potentially cause skin infections

For external use only

Do not use

• if allergic to iodine

• in the eyes

• on children less than 3 years old

A sk a doctor before use if injuries are

• deep or puncture wounds

• serious burns

Stop use and ask 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:

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

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

3. Using a second swab, repeat step 2 with the other nostril.

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

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

Other information

• 1% titratable iodine

• latex free

• for hospital or professional use only

Inactive ingredients

• disodium phosphate

• glycerin

• hydroxyethylcellulose

• nonoxynol-10

• simethicone

• water

For questions, comments, or to report serious side effects:

800-760-3236

Monday-Friday

8:30 a.m. - 5 p.m. EST

52380-0972CLOROX HEALTHCARE

Nasal Antiseptic Swabs

Povidone-Iodine 10%

Sterile Solution

CLOROX HEALTHCARE NASAL ANTISEPTIC SWABS 
povidone iodine swabstick solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52380-0972
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 CPS AT 1%) (UNII: S38J6RZN16)  
NONOXYNOL-10 (UNII: K7O76887AP)  
GLYCERIN (UNII: PDC6A3C0OX)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52380-0972-610 mL in 1 PACKET; Type 0: Not a Combination Product11/08/201507/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A11/08/201507/01/2020
Labeler - Aplicare Products, LLC. (081054904)
Establishment
NameAddressID/FEIBusiness Operations
Aplicare Products, LLC.081054904manufacture(52380-0972)

Revised: 1/2020
 
Aplicare Products, LLC.