FDA.reportPublic FDA data

Moxie Moisturizing Hand Sanitizer

Manufacturer
L G Sourcing, Inc.
Effective date
2020-03-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:38:10

Label at a glance#

ProductMoxie Moisturizing Hand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Indications and uses

To decrease bacteria on skin that could cause disease. Recommended for repeated use.

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

To decrease bacteria on skin that could cause disease.

Recommended for repeated use.

Warnings

WARNINGS SECTION

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

OTC - DO NOT USE SECTION

Do not use this product in or near eyes.

OTC - STOP USE SECTION

Stop use if irritation or redness develop. If conditions persist for more than 72 hours, consult a doctor.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, seek immediate medical attention or contact a Poison Control Center.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (aqua), glycerin, carbomer, triethanolamine, fragrance, glycereth-7 triacetate, alpha-tocopherol and denatonium benoate.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 73841-400-1

Moxie

Mosisturizing Hand Sanitizer

Kills germs in 30 Seconds

Kills 99.99% of Germs

Moxie LabelMoxie Label

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73841-40073841-400-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERETH-7 TRIACETATES9W6Z48HUPIACT
GLYCERINPDC6A3C0OXIACT
TROLAMINE9O3K93S3TKIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
.ALPHA.-TOCOPHEROL, D-N9PR3490H9IACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
DENATONIUM BENZOATE ANHYDROUSM5BA6GAF1OIACT

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
d320419e-570f-0510-e053-2a95a90aa9c6a21795c6-79cc-83ce-e053-2995a90a2d1a2021-12-14WarningsExact identifier
spl set id: a21795c6-79cc-83ce-e053-2995a90a2d1a

Reported adverse events (FAERS/openFDA)#

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