Alcohol Prep Pads

Manufacturer
Htl-Strefa, Inc.
Effective date
2025-10-23
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:40:39

Label at a glance#

ProductAlcohol Prep Pads
Active ingredientISOPROPYL ALCOHOL
Label structure11 sections

Dosage and administration

Wipe injection site vigorously.

Storage and handling

Store at Room Temperature

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For preparation of the skin prior to injection, to decrease germs in minor cuts and scrapes.

Warning

WARNINGS SECTION

For external use only. Flammable. Keep away from fire and flame.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center immediately.

Caution

OTHER SAFETY INFORMATION

Do not apply to irritated skin

Do not use

OTC - DO NOT USE SECTION

Do not use in the eyes, or on mucous membranes. In case of deep or puncture wounds, consult a doctor.

Directions

DOSAGE & ADMINISTRATION SECTION

Wipe injection site vigorously.

Other Information

STORAGE AND HANDLING SECTION

Store at Room Temperature

Inactive Ingredieent

INACTIVE INGREDIENT SECTION

Water

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Dropsafe IBDropsafe IB

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
797544isopropyl alcohol 70 % Medicated PadPSN5
797544isopropyl alcohol 0.7 ML/ML Medicated PadSCD5
797544isopropyl alcohol 70 % Medicated PadSY5
797544isopropyl alcohol 70 % Topical ClothSY5
797544isopropyl alcohol 70 % Topical SwabSY5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81603-625-10Alcohol Prep Pads1 mL in 1 PACKETSWAB15
81603-625-10Alcohol Prep Pads100 in 1 CARTONSWAB1005

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
81603-625-10EA - Each81603-625d5ea30fb-8074-46c8-a055-ba1a1c6d327512022-03-09

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81603-62581603-625-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
ISOPROPYL ALCOHOLND2M416302ACTIB
WATER059QF0KO0RIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
42024-10-17full-release2026-06-01 00:27:16

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
Alcohol Prep PadsISOPROPYL ALCOHOLHtl-Strefa, Inc.d72ddf5a-72e7-c37d-e053-2995a90ad48b2025-10-23WarningsExact identifier
ndc (package): 81603-625-10
ndc (product): 81603-625
ndc11 (package): 81603062510
spl id: 41d13ef7-8026-508b-e063-6294a90a4787
spl set id: d72ddf5a-72e7-c37d-e053-2995a90ad48b

Reported adverse events (FAERS/openFDA)#

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