Alcohol Prep - ARISE PHARMACEUTICALS LLC

Manufacturer
ARISE PHARMACEUTICALS LLC
Effective date
2015-09-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:30:40

Label at a glance#

ProductAlcohol Prep
Active ingredientISOPROPYL ALCOHOL
Label structure8 sections

Dosage and administration

Wipe injection site vigorously.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol USP, 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use:

INDICATIONS & USAGE SECTION

For preparation of the skin prior to injection

Warnings:

WARNINGS SECTION

  • For external use only. Flammable; keep away from fire and flame.

Do not use

OTC - DO NOT USE SECTION

in the eyes, or on mucous membranes. In case of deep or puncture wounds, consult a doctor.


Caution:

OTHER SAFETY INFORMATION

Do not apply to irritated skin.


Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a poison control center immediately.


Directions:

DOSAGE & ADMINISTRATION SECTION

Wipe injection site vigorously.


Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water


Other information:

SPL UNCLASSIFIED SECTION

Store at room temperature.


Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

100

ULTRA CARE

Alcohol Prep Pad

MEDIUM 2 - PLY PREP PAD

STERILIZED WITH GAMMA RADIATION

Latex Free



Untitled.jpg
Untitled.jpg



Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130369967002015GTIN-13: 0369967002015
EAN-13: 0369967002015
GTIN-12: 369967002015
UPC-A: 369967002015
GTIN storage (14 digits): 00369967002015
Untitled.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69967-002-012020-11-07C16284748780-19d75b9d0-4d4d-f424-e053-dadaa90a57ceDrug Facts
69967-002-012020-01-31C16284748780-19d75b9d0-4d4d-f424-e053-dadaa90a57ceDrug Facts

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ISOPROPYL ALCOHOLACTIVE INGREDIENTND2M4163021
ISOPROPYL ALCOHOLACTIVE MOIETYND2M4163021
WATERINACTIVE INGREDIENT059QF0KO0R1

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
69967-00269967-002-01

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
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302ACTIB

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
0b8d0f2c-31e8-41eb-b5c5-e04e497f45963f205fa5-f610-4e6c-91ce-760af8c071e82020-11-07WarningsExact identifier
spl set id: 3f205fa5-f610-4e6c-91ce-760af8c071e8

Reported adverse events (FAERS/openFDA)#

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