Hand Santizer

Product NDC: 74054-100
Requested package NDC: 74054-100-13
11-digit product format: 740540100
Labeler code: 74054
Product ID: 74054-100_a3d16c5e-5dac-7f57-e053-2a95a90a9a6f
Type: HUMAN OTC DRUG
Nonproprietary name: Alcohol
Dosage form: LIQUID
Route: TOPICAL
Labeler: Robert Mazza, Inc dba Five & 20 Spirits
Application: part333A
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2020-03-26
Marketing end: 0000-00-00
Substance: ALCOHOL
Active strength: 80 mL/100mL
NDC exclude flag: No
Listing certified through: 2021-12-31
Current FDA listing: Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	74054-100	74054-100-13	I	Inactivated by FDA		2026-10-05

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 18 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	`1332a3947898…`	`d4bfe170f9cd…`
2022-08-30 03:57 UTC · source 2022-08-29	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	`bd6a592717d7…`	`303034d00443…`

Reported adverse events (FAERS/openFDA)#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
5eb9f24b-9328-475e-af0a-18021935eb6a	Product name	1	20180220

FDA-Initiated Inactive NDC Indexing#

NDC, Indexing SPL, Related label table
NDC	Indexing SPL	Related label
74054-100-01	d6a99b39-ef43-a426-e053-dadaa90af4c2	a1c72256-8dd6-5b63-e053-2a95a90aba14
74054-100-02	d6a99b39-5498-a426-e053-dadaa90af4c2	a268e759-9a3f-1d7b-e053-2a95a90a335b
74054-100-03	d6a99b39-5498-a426-e053-dadaa90af4c2	a268e759-9a3f-1d7b-e053-2a95a90a335b
74054-100-04	d6a99b39-5498-a426-e053-dadaa90af4c2	a268e759-9a3f-1d7b-e053-2a95a90a335b
74054-100-05	d6a99b39-5498-a426-e053-dadaa90af4c2	a268e759-9a3f-1d7b-e053-2a95a90a335b
74054-100-06	d6a99b39-5498-a426-e053-dadaa90af4c2	a268e759-9a3f-1d7b-e053-2a95a90a335b
74054-100-07	d6a99b39-5498-a426-e053-dadaa90af4c2	a268e759-9a3f-1d7b-e053-2a95a90a335b
74054-100-08	d6a99b39-3ad1-a426-e053-dadaa90af4c2	a3d16ce9-1e9e-876d-e053-2a95a90af7b7
74054-100-09	d6a99b39-3ad1-a426-e053-dadaa90af4c2	a3d16ce9-1e9e-876d-e053-2a95a90af7b7
74054-100-10	d6a99b39-3ad1-a426-e053-dadaa90af4c2	a3d16ce9-1e9e-876d-e053-2a95a90af7b7
74054-100-11	d6a99b39-3ad1-a426-e053-dadaa90af4c2	a3d16ce9-1e9e-876d-e053-2a95a90af7b7
74054-100-12	d6a99b39-3ad1-a426-e053-dadaa90af4c2	a3d16ce9-1e9e-876d-e053-2a95a90af7b7
74054-100-13	d6a99b39-3ad1-a426-e053-dadaa90af4c2	a3d16ce9-1e9e-876d-e053-2a95a90af7b7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
74054-100-08	Hand Santizer	2018198 mL in 1 DRUM	LIQUID	2018198	3
74054-100-09	Hand Santizer	189271 mL in 1 DRUM	LIQUID	189271	3
74054-100-10	Hand Santizer	1893 mL in 1 BOTTLE, PLASTIC	LIQUID	1893	3
74054-100-11	Hand Santizer	250 mL in 1 BOTTLE, PLASTIC	LIQUID	250	3
74054-100-12	Hand Santizer	750 mL in 1 BOTTLE, PLASTIC	LIQUID	750	3
74054-100-13	Hand Santizer	591 mL in 1 BOTTLE, PLASTIC	LIQUID	591	3
74054-100-02	Hand Santizer	118 mL in 1 BOTTLE, PLASTIC	LIQUID	118	2
74054-100-03	Hand Santizer	237 mL in 1 BOTTLE, PLASTIC	LIQUID	237	2
74054-100-04	Hand Santizer	3785 mL in 1 BOTTLE, PLASTIC	LIQUID	3785	2
74054-100-05	Hand Santizer	18927 mL in 1 BOTTLE, PLASTIC	LIQUID	18927	2
74054-100-06	Hand Santizer	355 mL in 1 BOTTLE, PLASTIC	LIQUID	355	2
74054-100-07	Hand Santizer	473 mL in 1 BOTTLE, PLASTIC	LIQUID	473	2
74054-100-01	Hand Santizer	287 mL in 1 BOTTLE, PLASTIC	LIQUID	287	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
74054-100	HAND SANTIZER (ALCOHOL) LIQUID [ROBERT MAZZA, INC DBA FIVE & 20 SPIRITS]	3	Legacy NDC, 6 package rows	20200422_a3d16ce9-1e9e-876d-e053-2a95a90af7b7.zip
74054-100	HAND SANTIZER (ALCOHOL) LIQUID [ROBERT MAZZA, INC DBA FIVE & 20 SPIRITS]	2	Legacy NDC, 6 package rows	20200407_a268e759-9a3f-1d7b-e053-2a95a90a335b.zip
74054-100	HAND SANTIZER (ALCOHOL) LIQUID [ROBERT MAZZA, INC DBA FIVE & 20 SPIRITS]	1	Legacy NDC, 1 package rows	20200327_a1c72256-8dd6-5b63-e053-2a95a90aba14.zip

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
1039339	ethanol 80 % Topical Solution	PSN	a3d16ce9-1e9e-876d-e053-2a95a90af7b7	3
1039339	ethanol 0.8 ML/ML Topical Solution	SCD	a3d16ce9-1e9e-876d-e053-2a95a90af7b7	3
1039339	ethanol 80 % Topical Solution	SY	a3d16ce9-1e9e-876d-e053-2a95a90af7b7	3
1039339	ethanol 80 % Topical Solution	PSN	a268e759-9a3f-1d7b-e053-2a95a90a335b	2
1039339	ethanol 0.8 ML/ML Topical Solution	SCD	a268e759-9a3f-1d7b-e053-2a95a90a335b	2
1039339	ethanol 80 % Topical Solution	SY	a268e759-9a3f-1d7b-e053-2a95a90a335b	2
1039339	ethanol 80 % Topical Solution	PSN	a1c72256-8dd6-5b63-e053-2a95a90aba14	1
1039339	ethanol 0.8 ML/ML Topical Solution	SCD	a1c72256-8dd6-5b63-e053-2a95a90aba14	1
1039339	ethanol 80 % Topical Solution	SY	a1c72256-8dd6-5b63-e053-2a95a90aba14	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
74054-100-13	74054010013	591 mL in 1 BOTTLE, PLASTIC (74054-100-13)	591 ml	2020-03-26	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Hand Santizer - Robert Mazza, Inc dba Five & 20 Spirits \| Robert Mazza, Inc.	Robert Mazza, Inc dba Five & 20 Spirits \| Robert Mazza, Inc.	2020-04-21	HUMAN OTC DRUG LABEL	3
Hand Santizer - Robert Mazza, Inc dba Five & 20 Spirits \| Robert Mazza, Inc.	Robert Mazza, Inc dba Five & 20 Spirits \| Robert Mazza, Inc.	2020-04-03	HUMAN OTC DRUG LABEL	2
Hand Santizer - Robert Mazza, Inc dba Five & 20 Spirits \| Robert Mazza, Inc.	Robert Mazza, Inc dba Five & 20 Spirits \| Robert Mazza, Inc.	2020-03-26	HUMAN OTC DRUG LABEL	1