NDC- 63148-660

Manufacturer: Apollo Health and Beauty Care
Effective date: 2026-05-05
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-06-01 01:56:12

Label at a glance#

ProductMoxie

Active ingredientALCOHOL

Label structure9 sections

Indications and uses

For Personal hand hygiene to help the spread of bacteria. Can be used in place of hand washing if soap and water are not available.

Dosage and administration

For occasional and personal use Rub thoroughly into hands for at least 30 seconds. Allow to dry Children under 6 years should be supervised when using this product

Storage and handling

Store at a temperature below 110 0 F (43 0 C) May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol (70%)

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

For Personal hand hygiene to help the spread of bacteria. Can be used in place of hand washing if soap and water are not available.

Warnings

WARNINGS SECTION

For External use only
Flammable
Keep away from source of heat or fire.

When using this product

OTC - WHEN USING SECTION

Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water. Do not Inhale.

Do not use

OTC - DO NOT USE SECTION

on children less than 2 months of age
on open skin wounds
on broken or damaged skin

Stop use and ask a doctor

OTC - STOP USE SECTION

If Irritation or redness develops and lasts.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, get medical help or contact a Poison Control Centre immediately

Directions

DOSAGE & ADMINISTRATION SECTION

For occasional and personal use
Rub thoroughly into hands for at least 30 seconds. Allow to dry
Children under 6 years should be supervised when using this product

Other Information

STORAGE AND HANDLING SECTION

Store at a temperature below 110 ⁰F (43 ⁰C)
May discolor certain fabrics or surfaces

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), PEG-6, AMP-Acrylates/Vinyl Isodecanate Crosspolymer, Ethlylene Brassylate, Isopropyl Myristate, Glycerin, Isopropyl Alcohol, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice.

24 oz sanitizer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

24 oz sanitizer

50 oz sanitizer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50 oz sanitizer

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	4
581662	ethanol 0.7 ML/ML Topical Gel	SCD	4
581662	ethanol 70 % Topical Gel	SY	4
581662	ethyl alcohol 70 % Topical Gel	SY	4

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0670456968966	GTIN-13: 0670456968966 EAN-13: 0670456968966 GTIN-12: 670456968966 UPC-A: 670456968966 GTIN storage (14 digits): 00670456968966	24 oz sanitizer.jpg
Barcode	EAN-13	0670456968973	GTIN-13: 0670456968973 EAN-13: 0670456968973 GTIN-12: 670456968973 UPC-A: 670456968973 GTIN storage (14 digits): 00670456968973	50 oz sanitizer.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1	Product name	1	20230829

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
63148-660-24	Moxie	710 mL in 1 BOTTLE, PLASTIC	GEL	710		4
63148-660-50	Moxie	1470 mL in 1 BOTTLE, PLASTIC	GEL	1470		4

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

Moxie
Ethyl Alcohol
WATER
POLYETHYLENE GLYCOL 300
ISOPROPYL ALCOHOL
GLYCERIN
ISOPROPYL MYRISTATE
ALOE VERA LEAF
.ALPHA.-TOCOPHEROL ACETATE, DL-
ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%)
ETHYLENE BRASSYLATE
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
63148-660	63148-660-24, 63148-660-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
POLYETHYLENE GLYCOL 300	5655G9Y8AQ	IACT
ISOPROPYL ALCOHOL	ND2M416302	IACT
GLYCERIN	PDC6A3C0OX	IACT
ISOPROPYL MYRISTATE	0RE8K4LNJS	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
.ALPHA.-TOCOPHEROL ACETATE, DL-	WR1WPI7EW8	IACT
ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%)	2N8MDB79NA	IACT
ETHYLENE BRASSYLATE	9A87HC7ROD	IACT
ALCOHOL	3K9958V90M	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Moxie	ETHYL ALCOHOL	Apollo Health and Beauty Care	3752d034-d4b4-47ab-b1bb-066cef7fde75	2026-05-05	Warnings	Exact identifier ndc (package): 63148-660-24 ndc (package): 63148-660-50 ndc (product): 63148-660 ndc11 (package): 63148066024 ndc11 (package): 63148066050 spl id: 51177faa-2411-fc43-e063-6294a90ab0c7 spl set id: 3752d034-d4b4-47ab-b1bb-066cef7fde75

Reported adverse events (FAERS/openFDA)#

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