FDA.reportPublic FDA data

Grime STOPPERS Fast Acting Hand Sanitizer Gel

Manufacturer
EMCO Electric International
Effective date
2020-08-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:31:32

Label at a glance#

ProductGrime STOPPERS Fast Acting Hand Sanitizer Liquid
Active ingredientALCOHOL
Label structure10 sections

Dosage and administration

Apply to palm of your hands as needed. Rub hands together to spread gel until dry. No rinsing or towel required. Children under 6 years of age consult physician before use and supervise when using this product.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 80% v/v

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

USE

INDICATIONS & USAGE SECTION

Hand Sanitzer to help reduce bacteria on the skin that could cause disease or illness.

DOSAGE & ADMINISTRATION SECTION

Topical Liquid applied to outer surface of the body, specifcially hands.

WARNINGS

WARNINGS SECTION

  • For external use only.
  • Flammable. Keep away from fire or flame.

When using this product

OTC - WHEN USING SECTION

  • keep out of eyes, ears, and mouth. In case of contact, flush thoroughly with water.
  • Avoid contact with open wounds.
  • Do not ingest or inhale.

Stop us and ask a doctor

OTC - STOP USE SECTION

if irritation or rash appears and persists more than 72 hours.

Keep out of the reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS

INDICATIONS & USAGE SECTION

  • Apply to palm of your hands as needed. Rub hands together to spread gel until dry.
  • No rinsing or towel required.
  • Children under 6 years of age consult physician before use and supervise when using this product.

OTHER INFORMATION

OTHER SAFETY INFORMATION

  • Avoid freezing and store below 105°F (41°C).
  • May discolor or harm fabrics, wood finishes & plastics.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

  • Water
  • Glycerin
  • Hydrogen Peroxide
  • Biterex
  • Fragrance

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Liquid Application 1 Gallon (3.76L) NDC: 43636-007-28

63436-007-2863436-007-28

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Gel Application 1 Gallon (3.76L) NDC: 43636-008-28

63436-008-2863436-008-28

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1041498ethanol 80 % Topical GelPSN1
1039339ethanol 80 % Topical SolutionPSN1
1041498ethanol 0.8 ML/ML Topical GelSCD1
1039339ethanol 0.8 ML/ML Topical SolutionSCD1
1041498ethanol 80 % Topical GelSY1
1039339ethanol 80 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63436-007-282022-01-28C16284748780-1d6a99b39-7cdf-a426-e053-dadaa90af4c2Hand Sanitizer
63436-008-282022-01-28C16284748780-1d6a99b39-7cdf-a426-e053-dadaa90af4c2Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63436-007-28Grime STOPPERS Fast Acting Hand Sanitizer Liquid3760 mL in 1 JUGLIQUID37601
63436-008-28Grime STOPPERS Fast Acting Hand Sanitizer Gel3760 mL in 1 JUGGEL37601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63436-007GRIME STOPPERS FAST ACTING HAND SANITIZER LIQUID (ALCOHOL) LIQUID GRIME STOPPERS FAST ACTING HAND SANITIZER GEL (ALCOHOL) GEL [EMCO ELECTRIC INTERNATIONAL]1Legacy NDC, 1 package rows20201014_adf47e6a-3c2e-3e0b-e053-2a95a90a3122.zip
63436-008GRIME STOPPERS FAST ACTING HAND SANITIZER LIQUID (ALCOHOL) LIQUID GRIME STOPPERS FAST ACTING HAND SANITIZER GEL (ALCOHOL) GEL [EMCO ELECTRIC INTERNATIONAL]1Legacy NDC, 1 package rows20201014_adf47e6a-3c2e-3e0b-e053-2a95a90a3122.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
63436-00763436-007-28
63436-00863436-008-28

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
ALCOHOL3K9958V90MACTIB
DENATONIUM BENZOATE4YK5Z54AT2IACT
HYDROGEN PEROXIDEBBX060AN9VIACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
ALCOHOL3K9958V90MACTIB
DENATONIUM BENZOATE4YK5Z54AT2IACT
HYDROGEN PEROXIDEBBX060AN9VIACT
WATER059QF0KO0RIACT

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
adf47e6a-3c2f-3e0b-e053-2a95a90a3122adf47e6a-3c2e-3e0b-e053-2a95a90a31222020-08-28WarningsExact identifier
spl id: adf47e6a-3c2f-3e0b-e053-2a95a90a3122
spl set id: adf47e6a-3c2e-3e0b-e053-2a95a90a3122

Reported adverse events (FAERS/openFDA)#

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