Moxie Hand Sanitizing Gel

Product NDC: 77720-033
11-digit product format: 777200033
Labeler code: 77720
Product ID: 77720-033_2f69f248-b382-6811-e063-6394a90aa8a1
Type: HUMAN OTC DRUG
Nonproprietary name: Alcohol
Dosage form: GEL
Route: TOPICAL
Labeler: Skaffles Group
Marketing category: UNAPPROVED DRUG OTHER
Marketing start: 2024-05-15
Substance: ALCOHOL
Active strength: 71 mL/100mL
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Additional Listing Data#

Finished product: Yes
Brand name base: Moxie Hand Sanitizing Gel
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ALCOHOL	71 mL/100mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
3K9958V90M	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
2282911	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
fbb5cd9c-c9dc-42ed-9035-f57455ce092a	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
77720-033-01	Moxie Hand Sanitizing Gel	500 mL in 1 PACKAGE	GEL	500		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
77720-033	MOXIE HAND SANITIZING GEL (ALCOHOL) GEL [SKAFFLES GROUP]	3	Current NDC, 1 package rows	20250304_fbb5cd9c-c9dc-42ed-9035-f57455ce092a.zip

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 Hand Sanitizing Gel	ALCOHOL	Skaffles Group	fbb5cd9c-c9dc-42ed-9035-f57455ce092a	2025-03-02	Warnings	Exact identifier ndc (product): 77720-033

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
3K9958V90M	ALCOHOL	64-17-5	ALCOHOL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
2282911	ethanol 71 % Topical Gel	PSN	fbb5cd9c-c9dc-42ed-9035-f57455ce092a	3
2282911	ethanol 0.71 ML/ML Topical Gel	SCD	fbb5cd9c-c9dc-42ed-9035-f57455ce092a	3
2282911	ethanol 71 % Topical Gel	SY	fbb5cd9c-c9dc-42ed-9035-f57455ce092a	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
77720-033-01	77720003301	500 mL in 1 PACKAGE (77720-033-01)	500 ml	2024-05-15	No	No	Current