HandSanitizerStephanieYoung

Manufacturer
Genesis Salon Products | Cospro Development Corp
Effective date
2020-10-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:31:23

Label at a glance#

ProductHandSanitizerStephanieYoung
Active ingredientALCOHOL
Label structure13 sections

Dosage and administration

Put enough product in your palm to cover hands and rub together briskly until dry. Children under 6 years of age shoud be supervised when using this product.

Storage and handling

Store below 110F (43C) May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

This is a hand rub manufactured according to the Temporary Policy for Preparation of Certain Alcohol-Based Hand Rub Products During the Public Health Emergency (CoViD-19); Guidance for Industry.

The hand rub is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation) consistent with World Health Organization (WHO) recommendations:

  1. Alcohol (ethanol) 
  2. Glycerol
  3. Sterile distilled water.

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70%  Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Rub

Use

INDICATIONS & USAGE SECTION

Hand Sanitizerto help reduce bacteria on the skin

Warnings

WARNINGS SECTION

Flammable. Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

  • in or around eyes

OTC - WHEN USING SECTION

When using this product do not use in or near eyes. If contact occurs, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all drugs out of reach of children. If swallowed, get medical help or contact Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Put enough product in your palm to cover hands and rub together briskly until dry.
  • Children under 6 years of age shoud be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

  • Store below 110F (43C)
  • May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Deionized water, glycerin, polysorbate 20, aloe barbadensis leaf juice, orange peel oil, tocopheryl acetate, maltodextrin, parfum

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN1
582753ethanol 0.7 ML/ML Topical SolutionSCD1
582753ethanol 70 % Topical SolutionSY1
582753ethyl alcohol 70 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76650-122-012022-01-28C16284748780-1d6a99b39-fd6e-a426-e053-dadaa90af4c2c2973564-ea0e-47f6-a975-b7296a94f429

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76650-122-01HandSanitizerStephanieYoung59 mL in 1 BOTTLESOLUTION591

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76650-122HANDSANITIZERSTEPHANIEYOUNG (ALCOHOL) SOLUTION [GENESIS SALON PRODUCTS]1Legacy NDC, 1 package rows20201010_c2973564-ea0e-47f6-a975-b7296a94f429.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
76650-12276650-122-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
31593b52-0db4-4637-bc59-8f2868561cf6c2973564-ea0e-47f6-a975-b7296a94f4292020-10-09WarningsExact identifier
spl id: 31593b52-0db4-4637-bc59-8f2868561cf6
spl set id: c2973564-ea0e-47f6-a975-b7296a94f429

Reported adverse events (FAERS/openFDA)#

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