62% ETHYL ALCOHOL ANTISEPTIC NASAL- ethyl alcohol swab

62% Ethyl Alcohol Antiseptic Nasal by

Drug Labeling and Warnings

62% Ethyl Alcohol Antiseptic Nasal by is a Otc medication manufactured, distributed, or labeled by Medline Industries, LP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

Uses

 antiseptic skin preparation
 helps reduce bacteria that can
cause skin infections

Warnings

 for external use only

 flammable, keep away from open flame

Do not use

 in the eyes

 on children under 2 years of age unless directed by a doctor

Ask a doctor before use if injuries are

 deep or puncture wounds
 serious burns

Stop and ask a 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.

STORAGE AND HANDLING

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 right swab comfortably into right nostril and rotate for 30 seconds, covering all surfaces. Discard swabstick.

3. Use left swab, repeat step 2 with left nostril.

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

Other Information

- not made with natural rubber latex

- for hospital or professional use only

Inactive Ingredients

Ascorbyl Palmitate, Benzyl Alcohol, BHT,
Ricinus Communis (Castor) Seed Oil,
Glyceryl Laurate, Isopropyl Alcohol,
Menthol, Natural Fragrance,
Polyaminopropyl Biguanide,
Purified Water

SPL UNCLASSIFIED SECTION

Protect From Freezing,
Do not store above 105°F.
Temperature limits:
25°C-40°C

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

62% ETHYL ALCOHOL ANTISEPTIC NASAL 
ethyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53329-032
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERYL LAURATE (UNII: Y98611C087)
MENTHOL (UNII: L7T10EIP3A)
WATER (UNII: 059QF0KO0R)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
BENZYL ALCOHOL (UNII: LKG8494WBH)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
POLIHEXANIDE HYDROCHLORIDE (UNII: 4XI6112496)
ASCORBYL PALMITATE (UNII: QN83US2B0N)
CASTOR OIL (UNII: D5340Y2I9G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53329-032-78	6 mL in 1 PACKET; Type 0: Not a Combination Product	09/10/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/10/2019

Labeler - Medline Industries, Inc. (025460908)

Establishment
Name	Address	ID/FEI	Business Operations
Aplicare Products, LLC		081054904	manufacture(53329-032)