FDA.reportPublic FDA data

Pharmacys Prescription Hand Sanitizer

Manufacturer
American Consumer Products Corp
Effective date
2020-04-28
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:08:31

Label at a glance#

ProductPharmacys Prescription Hand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Directions - Apply directly onto hands, rub into skin until dry. Apply directly onto surfaces: knobs, handles, steering wheels, light swithches, grocery carts, countertops, etc and let air dry.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Active ingredients - Ethyl Alcohol 80%

Purpose

OTC - PURPOSE SECTION

Purpose - Antiseptic

Warnings

WARNINGS SECTION

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

Flammable. Keep away from fire or flame.

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

Indications & Usage

INDICATIONS & USAGE SECTION

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

Stop Use

OTC - STOP USE SECTION

Stop use and ask a 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 - Apply directly onto hands, rub into skin until dry. Apply directly onto surfaces: knobs, handles, steering wheels, light swithches, grocery carts, countertops, etc and let air dry.

Other Information

SPL UNCLASSIFIED SECTION

Other information - store at 20° C (68° to 77° F).

-may discolor fabrics.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: Purified Water (Aqua), Glycerin, Hydrogen Peroxide

Distributed By:

SPL UNCLASSIFIED SECTION

Distributed By:

American Consumer Products Corp

Vernon, CA 90058

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
1241663ethanol 80 % Topical SprayPSN3
1241663ethanol 0.8 ML/ML Topical SpraySCD3
1241663ethanol 80 % Topical SpraySY3

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72197-023-992021-07-23C16284748780-1c7ccaba7-0f3c-fd44-e053-dadaa90aa01bPharmacys Prescription Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72197-023-99Pharmacys Prescription Hand Sanitizer3785.41 mL in 1 BOTTLE, SPRAYSPRAY3785.413

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72197-023PHARMACYS PRESCRIPTION HAND SANITIZER (ALCOHOL) SPRAY [AMERICAN CONSUMER PRODUCTS CORP]3Legacy NDC, 1 package rows20200429_a38542a3-fa0f-3a3c-e053-2995a90a9689.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72197-02372197-023-99

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT
HYDROGEN PEROXIDEBBX060AN9VIACT

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
a461f480-60e1-90e5-e053-2a95a90a9c84a38542a3-fa0f-3a3c-e053-2995a90a96892020-04-28WarningsExact identifier
spl id: a461f480-60e1-90e5-e053-2a95a90a9c84
spl set id: a38542a3-fa0f-3a3c-e053-2995a90a9689

Reported adverse events (FAERS/openFDA)#

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