FDA.reportPublic FDA data

Pharmacys Prescription Hand Sanitizer

Manufacturer
American Consumer Products Corp
Effective date
2020-08-12
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:24:37

Label at a glance#

ProductPharmacys Prescription Hand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Indications and uses

Uses - Helps reduce bacteria on the skin that could cause disease. Recommended for repeated use.

Dosage and administration

Directions - apply as needed into your palms and thoroughly spread on both hands. Rub into skin until dry.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients - Ethyl Alcohol 65%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Uses - Helps reduce bacteria on the skin that could cause disease. Recommended for repeated use.

Warnings

WARNINGS SECTION

Warnings - For external use only. Do not ingest or swallow.

Flammable. Keep away from fire or flame.

Do not appy around eyes. Do not use in ears & mouth.

OTC - WHEN USING SECTION

When using this product, avoid contact with eyes. In case of contact, flush eyes with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

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

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 - apply as needed into your palms and thoroughly spread on both hands. Rub into skin until dry.

Other information

SPL UNCLASSIFIED SECTION

Other information - store at 20º C (68º to 77º F). May discolor fabrics.

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: Purified Water (Aqua), Carbomer, Aminomethyl Propanol, Tocopheryl Acetate (Vitamin E), Aloe Barbadensis (Aloe Vera) Leaf Juice

Pharmacys Prescription Hand Sanitizer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Pharmacys Prescription Hand SanitizerPharmacys Prescription Hand Sanitizer

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
902574ethanol 65 % Topical GelPSN3
902574ethanol 0.65 ML/ML Topical GelSCD3
902574ethyl alcohol 65 % Topical GelSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72197-028-962022-01-28C16284748780-1d6a99b39-7911-a426-e053-dadaa90af4c2Pharmacys Prescription Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72197-028-96Pharmacys Prescription Hand Sanitizer473 mL in 1 BOTTLEGEL4733

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72197-028PHARMACYS PRESCRIPTION HAND SANITIZER (ALCOHOL) GEL [AMERICAN CONSUMER PRODUCTS CORP]3Legacy NDC, 1 package rows20200813_acb7246c-e6ff-1e4c-e053-2995a90a2845.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72197-02872197-028-96

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
ALCOHOL3K9958V90MACTIB
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT

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
acb7239d-10e8-3881-e053-2a95a90ab5deacb7246c-e6ff-1e4c-e053-2995a90a28452020-08-12WarningsExact identifier
spl id: acb7239d-10e8-3881-e053-2a95a90ab5de
spl set id: acb7246c-e6ff-1e4c-e053-2995a90a2845

Reported adverse events (FAERS/openFDA)#

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