PHARMACYS PRESCRIPTION 8OZ HAND SANITIZER

Manufacturer
American Consumer Products Corp
Effective date
2025-01-23
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:53:35

Label at a glance#

ProductPHARMACYS PRESCRIPTION 8OZ HAND SANITIZER
Active ingredientALCOHOL
Label structure10 sections

Dosage and administration

Directions - pump 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 62%

Purpose

OTC - PURPOSE SECTION

Purpose: Antiseptic

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 swallow.

Flammable. Keep away from fire or flame.

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

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. If swallowed, get medical help or contact a Poison Control Center right away.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredients - water, triethanolamine, glycerin, propylene glycol, tocopheryl acetate, aloe barbadensis gel, carbomer, fragrance.

Directions

DOSAGE & ADMINISTRATION SECTION

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

Indications & Usage Section

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

Other Information

INSTRUCTIONS FOR USE SECTION

Other Information - store at 20o C (68o to 77o F).

- may discolor fabrics.

Pharmacy's Prescription 8 OZ Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Pharmacy's Prescription 8 OZ Hand SanitizerPharmacy's Prescription 8 OZ Hand Sanitizer

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN2
581660ethanol 0.62 ML/ML Topical GelSCD2
581660ethanol 62 % Topical GelSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72197-011-08PHARMACYS PRESCRIPTION 8OZ HAND SANITIZER237 mL in 1 BOTTLE, PUMPGEL2372

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72197-011PHARMACYS PRESCRIPTION 8OZ HAND SANITIZER (ALCOHOL) GEL [AMERICAN CONSUMER PRODUCTS CORP]2Current NDC, Legacy NDC, 1 package rows20250125_7a048607-f4c3-6724-e053-2a91aa0ab6f2.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
72197-01172197-011-08

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
PHARMACYS PRESCRIPTION 8OZ HAND SANITIZERALCOHOLAmerican Consumer Products Corp7a048607-f4c3-6724-e053-2a91aa0ab6f22025-01-23WarningsExact identifier
ndc (package): 72197-011-08
ndc (product): 72197-011
ndc11 (package): 72197001108
spl id: 2c697c30-8b5e-5b06-e063-6294a90aacea
spl set id: 7a048607-f4c3-6724-e053-2a91aa0ab6f2

Reported adverse events (FAERS/openFDA)#

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