Shimmy Neutral Hand Sanitizer

Manufacturer
Shimmy Products LLC
Effective date
2024-07-25
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:16:04

Label at a glance#

ProductShimmy Neutral Hand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

hand sanitizer to help reduce bacteria on the skin that could cause disease. for use when soap and water are not available

Dosage and administration

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

Storage and handling

Avoid freezing and excessive heat above 40ºC (104ºF). May discolor certain fabrics, materials or surfaces.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • hand sanitizer to help reduce bacteria on the skin that could cause disease.
  • for use when soap and water are not available

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from heat or flame.

Do not use

OTC - DO NOT USE SECTION

  • on children less than 2 months of age
  • on open skin wounds

When using this product

OTC - WHEN USING SECTION

  • keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or rash appears or lasts. These may be signs of a serious condition.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other information

STORAGE AND HANDLING SECTION

  • Avoid freezing and excessive heat above 40ºC (104ºF).
  • May discolor certain fabrics, materials or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, hyaluronic acid, aloe barbadensis leaf juice, fragrance, carbomer, sodium hydroxide.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SH25615ESH25615E

SH25623ESH25623E

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1020364ethanol 62 % Topical SprayPSN2
1020364ethanol 0.62 ML/ML Topical SpraySCD2
1020364ethanol 62 % Topical SpraySY2
1020364ethyl alcohol 62 % Topical SpraySY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81755-004-92Shimmy Neutral Hand Sanitizer236 mL in 1 CANSPRAY2362
81755-004-93Shimmy Neutral Hand Sanitizer266 mL in 1 CANSPRAY2662

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81755-004SHIMMY NEUTRAL HAND SANITIZER (ALCOHOL) SPRAY [SHIMMY PRODUCTS LLC]2Current NDC, Legacy NDC, 2 package rows20240726_df2761b9-0fca-5e2a-e053-2a95a90a9b8d.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81755-00481755-004-92, 81755-004-93

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
Shimmy Neutral Hand SanitizerALCOHOLShimmy Products LLCdf2761b9-0fca-5e2a-e053-2a95a90a9b8d2024-07-25WarningsExact identifier
ndc (package): 81755-004-92
ndc (package): 81755-004-93
ndc (product): 81755-004
ndc11 (package): 81755000493
ndc11 (package): 81755000492
spl id: 1e15674f-6d34-8007-e063-6294a90aedc2
spl set id: df2761b9-0fca-5e2a-e053-2a95a90a9b8d

Reported adverse events (FAERS/openFDA)#

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