MOXIE HAND SANITIZING GEL- alcohol gel

Moxie Hand Sanitizing Gel by

Drug Labeling and Warnings

Moxie Hand Sanitizing Gel by is a Otc medication manufactured, distributed, or labeled by Skaffles Group. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

Ethyl Alcohol 71% V/V

Purpose

Antiseptic

Use

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

Warnings

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

WHEN USING

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

STOP USE

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

KEEP OUT OF REACH OF CHILDREN

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

Directions

• 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

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

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

Inactive ingredients

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

QUESTIONS

Ditributed by: Lowe's Home Centers LLC

Mooresville NC 28117

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.

INGREDIENTS AND APPEARANCE

MOXIE HAND SANITIZING GEL 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77720-033
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	71 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
TROLAMINE (UNII: 9O3K93S3TK)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77720-033-01	500 mL in 1 PACKAGE; Type 0: Not a Combination Product	05/15/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/15/2024

Labeler - Skaffles Group (831115642)