FDA.reportPublic FDA data

Pharmacys Prescription Alcohol Wipes

Manufacturer
American Consumer Products Corp
Effective date
2020-08-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:24:49

Label at a glance#

ProductPharmacys Prescription Alcohol Wipes
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

Helps reduce bacteria on the skin that could cause disease.

Dosage and administration

Directions - Remove alcohol wipe from package. Thouroughly wipe skin, hands, fingers and wrists. Allow to dry. Discard after single use. Dispose of used alcohol wipes in trash receptacle. Do not flush.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients - Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Disinfectant

Uses

INDICATIONS & USAGE SECTION

Helps reduce bacteria on the skin that could cause disease.

Warnings

WARNINGS SECTION

Warnings - For external use only.

Flammable - Keep away from fire or flame.

Do not apply around eyes or use in ears & mouth.

When using this product

OTC - WHEN USING SECTION

When using this product, avoid contact with eyes.

In case of contact, flush eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

Strop use and ask doctor if redness or irritation develops and persists for more than 72 hours.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. Do not use on children less than 2 months of age. Supervise use in children under 6 years of age to prevent accidental swallowing. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions - Remove alcohol wipe from package. Thouroughly wipe skin, hands, fingers and wrists. Allow to dry. Discard after single use. Dispose of used alcohol wipes in trash receptacle. Do not flush.

Other Information

SPL UNCLASSIFIED SECTION

Other information - this is not a baby wipe - store at 20°C (68° to 77°F).

- may discolor fabrics

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS:

Water (Aqua), Aloe Essence Extract, Vitamin E, Phenoxyethanol, Sodium PCA, Benzalkonium Chloride, Sodium Carboxymethl Laurl Glucoside, Ethyl Glycerin, Cocamine DEA, Citric Acid

Distributed by

SPL UNCLASSIFIED SECTION

DISTRIBUTED BY:

American Consumer Products Corp.

VERNON, CA 90058

Made in China

Pharmacys Prescription Alcohol Wipes

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Alcohol Wipes 50 CountAlcohol Wipes 50 CountAlcohol Wipes 80 CountAlcohol Wipes 80 Count

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1307051ethanol 75 % Medicated PadPSN1
1307051ethanol 0.75 ML/ML Medicated PadSCD1
1307051ethanol 75 % Hand Sanitizer WipesSY1
1307051ethyl alcohol 75 % Topical ClothSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72197-031-502022-01-28C16284748780-1d6a99b39-e009-a426-e053-dadaa90af4c2Pharmacys Prescription Wipes
72197-031-802022-01-28C16284748780-1d6a99b39-e009-a426-e053-dadaa90af4c2Pharmacys Prescription Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72197-031-50Pharmacys Prescription Alcohol Wipes50 mL in 1 BAGSWAB501
72197-031-80Pharmacys Prescription Alcohol Wipes80 mL in 1 BAGSWAB801

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72197-031PHARMACYS PRESCRIPTION ALCOHOL WIPES (ALCOHOL) SWAB [AMERICAN CONSUMER PRODUCTS CORP]1Legacy NDC, 2 package rows20200815_acdd69e7-1225-c813-e053-2995a90ab4b1.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72197-03172197-031-50, 72197-031-80

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
PHENOXYETHANOLHIE492ZZ3TIACT
ETHYL GLYCERIN ACETAL LEVULINATE7233JH4G65IACT
COCO DIETHANOLAMIDE92005F972DIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
SODIUM PYRROLIDONE CARBOXYLATE469OTG57A2IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT
LAURYL GLUCOSIDE76LN7P7UCUIACT

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
acdd7406-9dab-235f-e053-2a95a90a2df7acdd69e7-1225-c813-e053-2995a90ab4b12020-08-14WarningsExact identifier
spl id: acdd7406-9dab-235f-e053-2a95a90a2df7
spl set id: acdd69e7-1225-c813-e053-2995a90ab4b1

Reported adverse events (FAERS/openFDA)#

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