Germ Nix Antibacterial Hand Sanitizer

Manufacturer
Lee's Collection Inc.
Effective date
2020-03-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:05:17

Label at a glance#

ProductGerm Nix Antibacterial Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Storage and handling

Other information  • Do not store above 105°F • May discolor some fabrics • Harmful to wood finish and plastics.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Ethyl alcohol 60%

OTC - PURPOSE SECTION

Purpose

Antiseptic

INDICATIONS & USAGE SECTION

Use • to decrease bacteria on the skin that could cause disease • recommended for repeated use.

WARNINGS SECTION

Warning

For external use only: Hands.

Flammable: keep away from fire and flame.

Use with caution for people with alcohol allergies.

When using this product • keep out of eyes. In case of contact with eyes, flush thoroughly with water • Avoid contact with broken skin. Do not inhale or ingest.

Stop use and ask a doctor if irritation and redness develop • and condition persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

Directions Wet hands thoroughly with product and allow to dry without wiping. For children under 6, use only under adult supervision. Not recommended for infants.

STORAGE AND HANDLING SECTION

Other information • Do not store above 105°F • May discolor some fabrics • Harmful to wood finish and plastics.

INACTIVE INGREDIENT SECTION

Inactive ingredients: Pure water, carbomer, glycerin, triethanolamine, and organic plant extract

SPL UNCLASSIFIED SECTION

Kills 99.99% of germs

Effective at eliminating over 99.99% of common harmful germs and bacteria in less than 15 seconds.

Distributed by • Perfect Hemp Organic Company S.EI Monte, CA 91733

EXP: 18 months after production date

Made in China

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581658ethanol 60 % Topical GelPSN1
581658ethanol 0.6 ML/ML Topical GelSCD1
581658ethanol 60 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74027-100-01Germ Nix Antibacterial Hand Sanitizer60 mL in 1 BOTTLE, PLASTICGEL601
74027-100-02Germ Nix Antibacterial Hand Sanitizer100 mL in 1 BOTTLE, PLASTICGEL1001
74027-100-03Germ Nix Antibacterial Hand Sanitizer250 mL in 1 BOTTLE, PLASTICGEL2501
74027-100-04Germ Nix Antibacterial Hand Sanitizer750 mL in 1 BOTTLE, PLASTICGEL7501
74027-100-05Germ Nix Antibacterial Hand Sanitizer1000 mL in 1 BOTTLE, PLASTICGEL10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74027-100GERM NIX ANTIBACTERIAL HAND SANITIZER (ETHYL ALCOHOL) GEL [LEE'S COLLECTION INC.]1Legacy NDC, 5 package rows20200408_31e9ecec-97bc-4b0d-91a9-11a67e45df06.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
74027-10074027-100-01, 74027-100-02, 74027-100-03, 74027-100-04, 74027-100-05

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
eb9417ea-810c-4cef-9d6b-90fe955bc52531e9ecec-97bc-4b0d-91a9-11a67e45df062020-03-28WarningsExact identifier
spl id: eb9417ea-810c-4cef-9d6b-90fe955bc525
spl set id: 31e9ecec-97bc-4b0d-91a9-11a67e45df06

Reported adverse events (FAERS/openFDA)#

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