SANIISWAB- ethyl alcohol 62% swab

SaniiSwab by

Drug Labeling and Warnings

SaniiSwab by is a Otc medication manufactured, distributed, or labeled by PolleyMed LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Step 2: Ethyl Alcohol 62%

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:

• 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.

Keep out of reach of children.

DOSAGE & ADMINISTRATION

Directions: 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
• Childen under 5 years: Ask a Doctor

OTHER SAFETY INFORMATION

• protect from excessive moisture

INACTIVE INGREDIENT

Step 1: Water, Glycerin, Sodium Chloride, Sodium Benzoate, PEG-60 Hydrogenated Castor Oil, Cocamidopropyl Betaine, Lavender Oil
Step 2: Water

OTHER SAFETY INFORMATION

■ Store between 5 C ( 41 F) and 40 C (104 F)

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SANIISWAB 
ethyl alcohol 62% swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87051-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.62 g  in 1 g

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87051-001-50	50 in 1 BOX	01/10/2025
1		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	01/10/2025

SANIISWAB 
ethyl alcohol 62% swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87051-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.62 g  in 1 g

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87051-002-10	10 in 1 BOX	09/01/2025
1		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	09/01/2025

Labeler - PolleyMed LLC (119559950)