PHARMACYS PRESCRIPTION HAND SANITIZER

Manufacturer
American Consumer Products Corp
Effective date
2021-07-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:44:34

Label at a glance#

ProductPHARMACYS PRESCRIPTION HAND SANITIZER
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

Directions: apply as needed in your palms, rub into skin until dry.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Purpose: Antiseptic

Uses - Reduces bacteria on skin that could cause disease.

Warnings

WARNINGS SECTION

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

Flammable. Keep away from fire or flame.

Stop Use

OTC - STOP USE SECTION

Stop use and ask a doctor if: 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. If swallowed, get medical help or contact a Poison Control Center right away.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredients - Glycerin, propylene glycol, triethanolamine, carbomer, fragrance, disodium edta, tocopheryl acetate, deionized water.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions: apply as needed in your palms, rub into skin until dry.

Indications & Usage Section

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

Pharmacy's Prescription Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Pharmacys Prescription Hand SanitizerPharmacys Prescription Hand Sanitizer

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2286295ethanol 75 % Topical SprayPSN1
2286295ethanol 0.75 ML/ML Topical SpraySCD1
2286295ethanol 75 % Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72197-035-102023-01-30C16284748780-1f386c649-aa87-0266-e053-dadaa90a7c1aPharmacy's Prescription Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72197-035-10PHARMACYS PRESCRIPTION HAND SANITIZER10 mL in 1 BOTTLE, SPRAYLIQUID101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72197-035PHARMACYS PRESCRIPTION HAND SANITIZER (ALCOHOL) LIQUID [AMERICAN CONSUMER PRODUCTS CORP]1Legacy NDC, 1 package rows20211030_c62b7fa0-5ad7-276c-e053-2995a90ade25.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72197-03572197-035-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

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
c62b7fa0-5ad8-276c-e053-2995a90ade25c62b7fa0-5ad7-276c-e053-2995a90ade252021-07-15WarningsExact identifier
spl id: c62b7fa0-5ad8-276c-e053-2995a90ade25
spl set id: c62b7fa0-5ad7-276c-e053-2995a90ade25

Reported adverse events (FAERS/openFDA)#

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