AZX Wellness Hand Sanitizer

Product NDC: 73145-007
11-digit product format: 731450007
Labeler code: 73145
Product ID: 73145-007_0b6dc42e-c0ac-b6cf-e063-6294a90aef5b
Type: HUMAN OTC DRUG
Nonproprietary name: ALCOHOL
Dosage form: GEL
Route: TOPICAL
Labeler: ASC Marketing LTD
Application: 505G(a)(3)
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2020-11-21
Substance: ALCOHOL
Active strength: .8 mL/mL
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: AZX Wellness Hand Sanitizer
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ALCOHOL	.8 mL/mL

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
1041498	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
b57c7e3a-f0bf-fd42-e053-2a95a90a3b4f	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73145-007-01	AZX Wellness Hand Sanitizer	3780 mL in 1 BOTTLE, PUMP	GEL	3780		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73145-007	AZX WELLNESS HAND SANITIZER (ALCOHOL) GEL [ASC MARKETING LTD]	2	Current NDC, Legacy NDC, 1 package rows	20231202_b57c7e3a-f0bf-fd42-e053-2a95a90a3b4f.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
AZX Wellness Hand Sanitizer	ALCOHOL	ASC Marketing LTD	b57c7e3a-f0bf-fd42-e053-2a95a90a3b4f	2023-12-01	Warnings	Exact identifier ndc (product): 73145-007

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
1041498	ethanol 80 % Topical Gel	PSN	b57c7e3a-f0bf-fd42-e053-2a95a90a3b4f	2
1041498	ethanol 0.8 ML/ML Topical Gel	SCD	b57c7e3a-f0bf-fd42-e053-2a95a90a3b4f	2
1041498	ethanol 80 % Topical Gel	SY	b57c7e3a-f0bf-fd42-e053-2a95a90a3b4f	2

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
73145-007-01	73145000701	3780 mL in 1 BOTTLE, PUMP (73145-007-01)	3780 ml	2020-11-21	0000-00-00	No	No	Current