FDA.reportPublic FDA data

GREASE MAGIC HAND SANIITIZER

Manufacturer
NU-TECH CLEANING SYSTEMS, INC.
Effective date
2022-01-26
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:47:38

Label at a glance#

ProductGREASE MAGIC HAND SANIITIZER
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 80% v/v.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can 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 if irritation or rash develop. these may be signs of serious condition and persist.

when using this product do not smoke

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control .

Inactive ingredients

INACTIVE INGREDIENT SECTION

Glycerin, Hydrogen peroxide, purified water USP

SPL UNCLASSIFIED SECTION

Other information

store between 15-30C(59-86F). Avoid freezing and excessive heat above 40C.

Keep away from open flame and heat. to avoid breathing vapors on mist open in well ventilated or outside places. if you experience
eye watering, headache dizziness, increase fresh air or wear respiratory protection or leave the area.

PRECAUTIONARY statements: do not smoke while using this product. do not use near open flames or while welding.

First aid: if swallowed do not induce vomiting do seek physician immediately in case of eye contact thoroughly wash eyes for up 10 15 minutes and seek a physician immediately.
notice: reports have associated repeated and prolonged occupational over exposure to certain solvents can be harmful possibly fatal.

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1041498ethanol 80 % Topical GelPSN3
1041498ethanol 0.8 ML/ML Topical GelSCD3
1041498ethanol 80 % Topical GelSY3

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
90064-001-012023-07-28C16284748780-10191ceaa-698a-198a-e063-dbdaa90aec3e0b702ba4-72eb-4e53-8d7c-908afe9c5580
90064-001-022023-07-28C16284748780-10191ceaa-698a-198a-e063-dbdaa90aec3e0b702ba4-72eb-4e53-8d7c-908afe9c5580
90064-001-032023-07-28C16284748780-10191ceaa-698a-198a-e063-dbdaa90aec3e0b702ba4-72eb-4e53-8d7c-908afe9c5580
90064-001-042023-07-28C16284748780-10191ceaa-698a-198a-e063-dbdaa90aec3e0b702ba4-72eb-4e53-8d7c-908afe9c5580
90064-001-052023-07-28C16284748780-10191ceaa-698a-198a-e063-dbdaa90aec3e0b702ba4-72eb-4e53-8d7c-908afe9c5580
90064-001-062023-07-28C16284748780-10191ceaa-698a-198a-e063-dbdaa90aec3e0b702ba4-72eb-4e53-8d7c-908afe9c5580

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
90064-001-01GREASE MAGIC HAND SANIITIZER236 mL in 1 BOTTLE, PLASTICGEL2363
90064-001-02GREASE MAGIC HAND SANIITIZER473 mL in 1 BOTTLE, PLASTICGEL4733
90064-001-03GREASE MAGIC HAND SANIITIZER946 mL in 1 BOTTLE, PLASTICGEL9463
90064-001-04GREASE MAGIC HAND SANIITIZER3785 mL in 1 BOTTLE, PLASTICGEL37853
90064-001-05GREASE MAGIC HAND SANIITIZER208198 mL in 1 DRUMGEL2081983
90064-001-06GREASE MAGIC HAND SANIITIZER1040990 mL in 1 CONTAINERGEL10409903

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
90064-001GREASE MAGIC HAND SANIITIZER (ALCOHOL) GEL [NU-TECH CLEANING SYSTEMS, INC.]3Legacy NDC, 6 package rows20220127_0b702ba4-72eb-4e53-8d7c-908afe9c5580.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
90064-00190064-001-01, 90064-001-02, 90064-001-03, 90064-001-04, 90064-001-05, 90064-001-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

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

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
d68392ef-2119-6bb8-e053-2a95a90a2d180b702ba4-72eb-4e53-8d7c-908afe9c55802022-01-26WarningsExact identifier
spl id: d68392ef-2119-6bb8-e053-2a95a90a2d18
spl set id: 0b702ba4-72eb-4e53-8d7c-908afe9c5580

Reported adverse events (FAERS/openFDA)#

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