FDA.reportPublic FDA data

62% Ethyl Alcohol Nasal Swab

Manufacturer
IIMED MEDICAL MEXICANA S DE RL DE CV
Effective date
2024-02-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:11:48

Label at a glance#

Product62% Ethyl Alcohol Nasal Swab
Active ingredientDEHYDRATED ALCOHOL
Label structure8 sections

Indications and uses

helps reduce bacteria that can cause skin infections

Dosage and administration

Nasal Application: 1. Use a tissue to clean inside both nostrils, including inside tip of nostil. Discard. 2. Insert right swab comfortable into right nostil and rotate for 30 seconds, covering all surfaces. Discard swab. 3. Using left 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

Uses

INDICATIONS & USAGE SECTION

helps reduce bacteria that can cause skin infections

Warnings

WARNINGS SECTION

For external use only.

flammable, keep away from open 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 doctor before use if injuries are

OTC - ASK DOCTOR SECTION

-deep or puncture wounds

-serious burns

Stop use and ask doctor if

OTC - STOP USE SECTION

-redness, irritation, swelling or pain persists or increase

-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

Nasal Application:

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

2. Insert right swab comfortable into right nostil and rotate for 30 seconds, covering all surfaces. Discard swab.

3. Using left 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

-Store at room temperature

-not made with natural rubber latex

-for hospital or professional use only

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Entire LabelEntire Label

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
83062-03283062-032-29, 83062-032-78
53329-032

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
ISOPROPYL ALCOHOLND2M416302IACT
CASTOR OILD5340Y2I9GIACT
DEHYDRATED ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
POLYAMINOPROPYL BIGUANIDEDT9D8Z79ETIACT
ASCORBYL PALMITATEQN83US2B0NIACT
MENTHOLL7T10EIP3AIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
BENZYL ALCOHOLLKG8494WBHIACT

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
28ecf869-dd10-707d-e063-6394a90a479e07c2aaf3-57a1-1679-e063-6294a90a3a612024-12-10WarningsExact identifier
spl set id: 07c2aaf3-57a1-1679-e063-6294a90a3a61

Reported adverse events (FAERS/openFDA)#

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