FDA.reportPublic FDA data

62% Ethyl Alcohol Antiseptic Nasal

Manufacturer
Medline Industries, LP
Effective date
2024-07-09
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
legacy-cache
Hydrated at
2026-08-01 20:59:24

Label at a glance#

Product62% Ethyl Alcohol Antiseptic Nasal
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

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.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

  • helps reduce bacteria that can cause skin infections

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

  • in the eyes
  • on children under 2 years of age unless directed by a doctor

Ask a doctor before use if injuries are

OTC - ASK DOCTOR SECTION

  • deep or puncture wounds
  • serious burns

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • redness, irritation, swelling or pain persists or increases
  • infection occurs

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, seek professional assistance or consult a poison control center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

label directionslabel 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

OTHER SAFETY 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

INACTIVE INGREDIENT SECTION

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

Manufacturing Information

SPL UNCLASSIFIED SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label Front V2 RK23HNDLabel Front V2 RK23HND

Label Back V2 RK23HNDLabel Back V2 RK23HND

Label Box V2 RK23HNDLabel Box V2 RK23HND

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
53329-13253329-132-78, 53329-132-29

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
ASCORBYL PALMITATEQN83US2B0NIACT
CASTOR OILD5340Y2I9GIACT
ISOPROPYL ALCOHOLND2M416302IACT
BENZYL ALCOHOLLKG8494WBHIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
MENTHOLL7T10EIP3AIACT
WATER059QF0KO0RIACT
POLYAMINOPROPYL BIGUANIDEDT9D8Z79ETIACT

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
1cd5197e-d0a8-44c0-e063-6394a90a74aaa38038e0-2c68-ef44-e053-2a95a90a8a062024-07-09WarningsExact identifier
spl id: 1cd5197e-d0a8-44c0-e063-6394a90a74aa
spl set id: a38038e0-2c68-ef44-e053-2a95a90a8a06

Reported adverse events (FAERS/openFDA)#

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