Karens Sunshine

Manufacturer
QuickCo, LTD
Effective date
2020-07-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:26:38

Label at a glance#

ProductKarens Sunshine
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Use proper hand washing technique, if possible Place enough product on hands to cover all surfaces Rub hands together until dry

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

70% Ethyl Alcohol

Purpose

OTC - PURPOSE SECTION

Hand Sanitizer/Hand Wash/Antibacterial

Warnings

WARNINGS SECTION

  • For external use only
  • Flammable, keep away from flames or heat source
  • When using product, keep away from eyes and face
  • Keep out of reach of children
  • Discontinue use if irritation or redness develops
  • If swallowed, seek medical help or contact poison control right away
  • Do not store product above 100º F

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Aloe Vera, Glycerin, Hydrogen Peroxide

Directions

DOSAGE & ADMINISTRATION SECTION

  • Use proper hand washing technique, if possible
  • Place enough product on hands to cover all surfaces
  • Rub hands together until dry

Purpose

INDICATIONS & USAGE SECTION

Hand Sanitizer/Hand Wash/Antibacterial

Back Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Back PanelBack Panel

Front Display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front PanelFront Panel

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
79645-402-012021-07-23C16284748780-1c7ccaba7-2385-fd44-e053-dadaa90aa01baa8faff1-82ad-6071-e053-2a95a90adf40

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79645-402-01Karens Sunshine1 mL in 1 BOTTLE, DISPENSINGLIQUID11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79645-402KARENS SUNSHINE (ETHYL ALCOHOL HAND SANITIZER) LIQUID [QUICKCO, LTD]1Legacy NDC, 1 package rows20200903_aa8faff1-82ad-6071-e053-2a95a90adf40.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
79645-40279645-402-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
aa8faff1-82ae-6071-e053-2a95a90adf40aa8faff1-82ad-6071-e053-2a95a90adf402020-07-16WarningsExact identifier
spl id: aa8faff1-82ae-6071-e053-2a95a90adf40
spl set id: aa8faff1-82ad-6071-e053-2a95a90adf40

Reported adverse events (FAERS/openFDA)#

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