Label: POLLEYSWAB- alcohol liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

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.

Drug Label Information

Updated September 6, 2023

If you are a consumer or patient please visit this version.

View All Sections
  • ACTIVE INGREDIENT

    alcohol 65%

  • INACTIVE INGREDIENT

    Water, Glycerin, Sodium Chloride, lavender oil, coco-betaine, sodium benzoate

  • PURPOSE

    two-step method to clean and sanitize the skin
    of the inner nostrils
    ■ protect from excessive moisture
    ■ Avoid freezing and excessive heat above 40° C (104° F)
    Inactive Ingredients
    ■ cleans ■ sanitizes

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

  • INDICATIONS & USAGE

    Adults and children over 12 years of age
    Step 1. Cleaning. Open Step 1 packet and hold handle, inserting
    one swab tip into each nostril. Swab lower interior lining inside the
    nose in a circular motion 7 times. Handle guard protects against
    insertion of swab tip beyond the nostrils. Discard.
    Step 2. Sanitizing. Repeat Step 1 with Step 2 packet. Discard

  • WARNINGS

    Flammable, keep away from fire and flames
    For external use only

  • DOSAGE & ADMINISTRATION

    For external use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    POLLEYSWAB 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77039-023
    Route of AdministrationNASAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL65 mL  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77039-023-010.3 g in 1 POUCH; Type 0: Not a Combination Product05/03/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A05/03/2023
    Labeler - IDO PHARM (694853523)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!