Moxie Hand Sanitizing Gel

Manufacturer
Skaffles Group
Effective date
2025-03-02
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:56:30

Label at a glance#

ProductMoxie Hand Sanitizing Gel
Active ingredientALCOHOL
Label structure13 sections

Dosage and administration

Pump a small amount in your palm and briskly rub hands together until dry. Children under 6 years of age should be supervised when in use.

Storage and handling

Store between 15-30C (59-89F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 71% V/V

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

  • for hand sanitizing to decrease bacteria on the skin
  • recommended for repeated use

Warnings

WARNINGS SECTION

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

OTC - WHEN USING SECTION

When using this productdo not use in or near the eyes. In case of contact, rinse eyes thoroughly with water

OTC - STOP USE SECTION

Discontinue Use if irritation and redness develop. If condition persists for more than 72 hours consult a doctor

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Pump a small amount in your palm and briskly rub hands together until dry.
  • Children under 6 years of age should be supervised when in use.

Other Information

STORAGE AND HANDLING SECTION

Store between 15-30C (59-89F)

Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Carbomer, Triethanolamine, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate (Vitamin E).

OTC - QUESTIONS SECTION

Ditributed by: Lowe's Home Centers LLC

Mooresville NC 28117

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Moxie

HAND SANITIZER GEL

Kills 99.9% of most common germs

Moisturizes with Aloe & Vitamin E

Light & Fresh Scent

16.9 FL OZ (500ml)

MADE IN CHINA

Item

Model

MOXIE and logo deisign are trademarks or registered trademarks of LF, LLC. All rights reserved.

Lowes Sanitizer GelLowes Sanitizer Gel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2282911ethanol 71 % Topical GelPSN3
2282911ethanol 0.71 ML/ML Topical GelSCD3
2282911ethanol 71 % Topical GelSY3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77720-033-01Moxie Hand Sanitizing Gel500 mL in 1 PACKAGEGEL5003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77720-033MOXIE HAND SANITIZING GEL (ALCOHOL) GEL [SKAFFLES GROUP]3Current NDC, 1 package rows20250304_fbb5cd9c-c9dc-42ed-9035-f57455ce092a.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
77720-03377720-033-01

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
Moxie Hand Sanitizing GelALCOHOLSkaffles Groupfbb5cd9c-c9dc-42ed-9035-f57455ce092a2025-03-02WarningsExact identifier
ndc (package): 77720-033-01
ndc (product): 77720-033
ndc11 (package): 77720003301
spl id: 2f69f248-b382-6811-e063-6394a90aa8a1
spl set id: fbb5cd9c-c9dc-42ed-9035-f57455ce092a

Reported adverse events (FAERS/openFDA)#

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