Medline

Manufacturer
Medline Industries, LP
Effective date
2025-11-06
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:42:28

Label at a glance#

ProductMedline
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

helps reduce bacteria that potentially can cause skin infections

Dosage and administration

Swab locally as needed.

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 potentially 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 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

Swab locally as needed.

Other information

OTHER SAFETY INFORMATION

  • not made with natural rubber latex
  • for hospital or professional use only
  • protect from freezing, avoid excessive heat
  • do not store above 105˚F.
  • temperature limits: 25˚C-40˚C

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

Manufacturer Information

SPL UNCLASSIFIED SECTION

www.medline.com

©2024 Medline Industries, LP

Manufactured by: Medline Industries, LP,

Three Lakes Drive, Northfield, IL 60093 USA.

1-800-MEDLINE

REF: MDS1971

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1041780ethanol 62 % Medicated PadPSN3
1041780ethanol 0.62 ML/ML Medicated PadSCD3
1041780ethanol 62 % Hand Sanitizer WipesSY3
1041780ethanol 62 % Medicated PadSY3
1041780ethanol 62 % Topical ClothSY3
1041780ethanol 62 % Topical SwabSY3

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53329-121-09Medline1 in 1 POUCHSWAB13
53329-121-09Medline6 mL in 1 APPLICATORSWAB63
53329-121-29Medline1 in 1 POUCHSWAB13
53329-121-29Medline50 in 1 BOXSWAB503

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
53329-12153329-121-09, 53329-121-29

Ingredients#

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

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

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22024-07-01full-release2026-06-01 00:14:57

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
MedlineETHYL ALCOHOLMedline Industries, LP11fcc7e7-dfae-ee7d-e063-6294a90a3b312025-11-06WarningsExact identifier
ndc (package): 53329-121-09
ndc (package): 53329-121-29
ndc (product): 53329-121
ndc11 (package): 53329012129
ndc11 (package): 53329012109
spl id: 42f0f55d-fdf0-bc53-e063-6394a90accce
spl set id: 11fcc7e7-dfae-ee7d-e063-6294a90a3b31

Reported adverse events (FAERS/openFDA)#

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