FDA.reportPublic FDA data

Alcohol Prep Pads

Manufacturer
Raya Pharmaceuticals LLC
Effective date
2023-10-27
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-05-31 23:58:22

Label at a glance#

ProductAlcohol Prep Pads
Active ingredientISOPROPYL ALCOHOL
Label structure11 sections

Dosage and administration

Wipe injection site vigorously and discard

Storage and handling

Store at room temperature Protect from freezing. Avoid excessive heat.

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

For the preparation of the skin prior to an injection

Wipe injection site vigorously and discard

Alcohol SwabAlcohol Swab

PRECAUTIONS SECTION

- For external use only
- Flammable, keep away from fire or flame

WARNINGS AND PRECAUTIONS SECTION

Warnings

· For external use only
· Flammable, keep away from fire or flame

Stop Use

· If irritation and redness develop.
· If the condition persists consult your health care practitioner.

· Keep out of reach of children. If swallowed get medical help or contact a Poison Control Center right away.

STORAGE AND HANDLING SECTION

Store at room temperature

Protect from freezing. Avoid excessive heat.

Dosage and Administration

DOSAGE & ADMINISTRATION SECTION

Wipe injection site vigorously and discard

WARNINGS SECTION

For External Use

Flamable, Keep Away from fire and flame

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water

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 center right away.

Purpose section

OTC - PURPOSE SECTION

Use for preperation of the skin prioir to an injection

Isopropyl Alcohol 70%........................Purpose: Antiseptic

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70%........................Antiseptic

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ALCOHOL PREP PAD

Saturated with 70% Isopropyl Alcohol

100 Swabs

For External use only

Principal Display ImagePrincipal Display Image

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
797544isopropyl alcohol 70 % Medicated PadPSN6
797544isopropyl alcohol 0.7 ML/ML Medicated PadSCD6
797544isopropyl alcohol 70 % Medicated PadSY6
797544isopropyl alcohol 70 % Topical ClothSY6
797544isopropyl alcohol 70 % Topical SwabSY6

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82098-814-10Alcohol Prep Pads0.7 mL in 1 POUCHSWAB0.76

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82098-814ALCOHOL PREP PADS (70%ISOPROPYL ALCOHOL) SWAB [RAYA PHARMACEUTICALS LLC]6Current NDC, Legacy NDC, 1 package rows20231030_da108e12-4327-db1c-e053-2a95a90a211b.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
82098-814-10EA - Each82098-814c06b72e4-e47a-4d90-9622-7a63b41b456412024-12-10

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82098-81482098-814-10

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

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 Pads70%ISOPROPYL ALCOHOLRaya Pharmaceuticals LLCda108e12-4327-db1c-e053-2a95a90a211b2023-10-27WarningsExact identifier
ndc (package): 82098-814-10
ndc (product): 82098-814
ndc11 (package): 82098081410
spl id: 08b3fb58-1f79-d17b-e063-6294a90a5850
spl set id: da108e12-4327-db1c-e053-2a95a90a211b

Reported adverse events (FAERS/openFDA)#

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