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% v/v

Purpose

Antiseptic

Use

• helps reduce bacteria that can cause skin infections

Warnings

For external use only. Flammable. Keep away from heat or 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 use 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.

Directions

1. Use a tissue to clean the inside of both nostrils, including the inside tip of nostril. Discard.

2. Insert swab comfortably into right nostril and rotate for 30 seconds, covering all surfaces.

3. Using same 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
• protect from freezing, do not store above 105ºF
• temperature limits: 25ºC-40ºC

Inactive ingredients

ascorbyl palmitate, benzyl alcohol, BHT, ricinus communis (castor) seed oil, isopropyl alcohol, menthol, fragrance, polyaminopropyl biguanide, purified water

Manufacturing Information

Manufactured by:

Medline Industries, LP

Three Lakes Drive, Northfield, IL 60093 USA

www.medline.com

1-800-MEDLINE (633-5463)

REF: MDS1971

V2 RK23HND

Package Label

INGREDIENTS AND APPEARANCE

62% ETHYL ALCOHOL ANTISEPTIC NASAL 
ethyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53329-132
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
ASCORBYL PALMITATE (UNII: QN83US2B0N)
CASTOR OIL (UNII: D5340Y2I9G)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
BENZYL ALCOHOL (UNII: LKG8494WBH)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
MENTHOL (UNII: L7T10EIP3A)
WATER (UNII: 059QF0KO0R)
POLYAMINOPROPYL BIGUANIDE (UNII: DT9D8Z79ET)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53329-132-29	50 in 1 BOX	05/01/2020	01/01/2025
1	NDC: 53329-132-78	6 mL in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 53329-132-78	6 mL in 1 PACKET; Type 0: Not a Combination Product	05/01/2020	01/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	05/01/2020	01/01/2025

Labeler - Medline Industries, LP (025460908)

Registrant - Medline Industries, LP (025460908)