SaniiSwab

Manufacturer
POLLEY MED LLC
Effective date
2025-01-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:51:47

Label at a glance#

ProductSaniiSwab
Active ingredientALCOHOL
Label structure10 sections

Storage and handling

Protect from excessive moisture Avoid freezing and excessive heat above 40 °C (104 °F)

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Alcohol 62%. Purpose: Antiseptic

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

Two-step method to clean and sanitize the skin of the lower inner nostrils

■ cleans ■ sanitizes

WARNINGS SECTION

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

OTC - DO NOT USE SECTION

Do Not Use:

  • In eyes or mouth
  • More than twice a day
  • If product is opened or damaged
  • If you are allergic to any ingredients
  • If you have a history of nasal irritation or bleeding

Stop use and ask a doctor if redness, pain, or irritation appear and lasts more than 24 hours. Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

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 skin 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.


Adults and children 12 years and over- Use once a day
Children under 12 years of age- Use under adult supervision
Children under 5 years- Ask a doctor

STORAGE AND HANDLING SECTION

  • Protect from excessive moisture
  • Avoid freezing and excessive heat above 40 °C (104 °F)

INACTIVE INGREDIENT SECTION

water, glycerin, sodium chloride, sodium benzoate, PEG-60 hydrogenated castor oil, cocamidopropyl betaine, lavender oil

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package labelPackage label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1041780ethanol 62 % Medicated PadPSN1
1041780ethanol 0.62 ML/ML Medicated PadSCD1
1041780ethanol 62 % Hand Sanitizer WipesSY1
1041780ethanol 62 % Medicated PadSY1
1041780ethanol 62 % Topical ClothSY1
1041780ethanol 62 % Topical SwabSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84456-746-01SaniiSwab0.3 g in 1 PACKETSWAB0.31
84456-746-02SaniiSwab100 in 1 BOXSWAB1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84456-746SANIISWAB (ETHYL ALCOHOL) SWAB [POLLEY MED LLC]1Current NDC, 2 package rows20250112_2ad08239-18ea-9ec9-e063-6394a90a3a54.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84456-74684456-746-01, 84456-746-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SaniiSwabETHYL ALCOHOLPOLLEY MED LLC2ad08239-18ea-9ec9-e063-6394a90a3a542025-01-10WarningsExact identifier
ndc (package): 84456-746-01
ndc (package): 84456-746-02
ndc (product): 84456-746
ndc11 (package): 84456074602
ndc11 (package): 84456074601
spl id: 2ad08239-18eb-9ec9-e063-6394a90a3a54
spl set id: 2ad08239-18ea-9ec9-e063-6394a90a3a54

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.