SANIISWAB- isopropyl alcohol swab

Saniiswab by

Drug Labeling and Warnings

Saniiswab by is a Otc medication manufactured, distributed, or labeled by POLLEY MED LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Isopropyl alcohol 70%. Purpose: Antiseptic

PURPOSE

Antiseptic

INDICATIONS & USAGE

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

WARNINGS

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

DO NOT USE

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

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

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

INACTIVE INGREDIENT

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

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SANIISWAB 
isopropyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84456-026
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	0.7 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
PEG-60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM BENZOATE (UNII: OJ245FE5EU)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
WATER (UNII: 059QF0KO0R)
LAVENDER OIL (UNII: ZBP1YXW0H8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84456-026-02	100 in 1 BOX	03/20/2025
1	NDC: 84456-026-01	0.3 g in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	03/20/2025

Labeler - POLLEY MED LLC (125097794)