Scullys Hand Sanity Hand Sanitizer

Manufacturer
Scully's Wonderful Stuff Inc.
Effective date
2020-04-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:35:08

Label at a glance#

ProductScullys Hand Sanity Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Sanitizer to help decrease bacteria on skin & surfaces. Recommended for repeated use.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses:

INDICATIONS & USAGE SECTION

Sanitizer to help decrease bacteria on skin & surfaces. Recommended for repeated use.

Warnings:

WARNINGS SECTION

Flammable. Keep away from Fire or Flame

For External Use Only.

  • When using this product, avoid contact with the eyes. In case of contact flush eyes with water.
  • Stop use and consult a doctor if redness or irritation develops and persists.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Keep out of reach of children
  • Children should be supervised when using this product

-As Scully would say, "Use your noggin!"

DOSAGE & ADMINISTRATION SECTION

Directions for hands: Spritz 5+ times on hands and fingertips. Rub hands together briskly until dry.

Directions for surfaces: Cover surface thoroughly and wipe with clean cloth or tissue. For more tips visit scullysworks.com

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, organic mint & sage oils, organic cucumber

Questions or Comments?

OTC - QUESTIONS SECTION

917-941-2243 Mon-Fri 9-5PM EST

info@scullyswonderfulstuff.com

SPL UNCLASSIFIED SECTION

SINCE 1928

Refill

HAND & PHONE SANITIZER

FAMILY OWNED • BROOKLYN, NY

Scully's​TM​ and Hand Sanity​TM

are trademarks of

Scully's Wonderful Stuff Inc.

Manufactured & Bottled by

Scully's Wonderful Stuff

456 Myrtle Ave

Brooklyn, NY, 11205

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sanity1Sanity1

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73958-00173958-001-01

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
79cf2a3e-1ab4-4bc7-ae81-394366638456e58ca448-d7cd-4e23-af7d-caf9f0e1f5272023-01-27WarningsExact identifier
spl set id: e58ca448-d7cd-4e23-af7d-caf9f0e1f527

Reported adverse events (FAERS/openFDA)#

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