MU instant hand sanitizer

Product NDC: 78422-001
Requested package NDC: 78422-001-12
11-digit product format: 784220001
Labeler code: 78422
Product ID: 78422-001_0e81daa3-f92e-4c1b-9ee5-12a1dd1de81e
Type: HUMAN OTC DRUG
Nonproprietary name: Alcohol
Dosage form: GEL
Route: TOPICAL
Labeler: Ningbo Royal Union Co., Ltd.
Application: part333A
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2020-05-20
Marketing end: 0000-00-00
Substance: ALCOHOL
Active strength: 75 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	78422-001	78422-001-12	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.

FDA-Initiated Inactive NDC Indexing#

NDC, Related label table
NDC	Related label
78422-001-01	73283c83-2cdf-48cb-a08c-328bfeae1b89
78422-001-02	73283c83-2cdf-48cb-a08c-328bfeae1b89
78422-001-03	73283c83-2cdf-48cb-a08c-328bfeae1b89
78422-001-04	73283c83-2cdf-48cb-a08c-328bfeae1b89
78422-001-05	73283c83-2cdf-48cb-a08c-328bfeae1b89
78422-001-06	73283c83-2cdf-48cb-a08c-328bfeae1b89
78422-001-07	73283c83-2cdf-48cb-a08c-328bfeae1b89
78422-001-08	73283c83-2cdf-48cb-a08c-328bfeae1b89
78422-001-09	73283c83-2cdf-48cb-a08c-328bfeae1b89
78422-001-10	73283c83-2cdf-48cb-a08c-328bfeae1b89
78422-001-11	73283c83-2cdf-48cb-a08c-328bfeae1b89
78422-001-12	73283c83-2cdf-48cb-a08c-328bfeae1b89
78422-001-13	73283c83-2cdf-48cb-a08c-328bfeae1b89
78422-001-14	73283c83-2cdf-48cb-a08c-328bfeae1b89
78422-001-15	73283c83-2cdf-48cb-a08c-328bfeae1b89
78422-001-16	73283c83-2cdf-48cb-a08c-328bfeae1b89
78422-001-17	73283c83-2cdf-48cb-a08c-328bfeae1b89
78422-001-18	73283c83-2cdf-48cb-a08c-328bfeae1b89
78422-001-19	73283c83-2cdf-48cb-a08c-328bfeae1b89
78422-001-20	73283c83-2cdf-48cb-a08c-328bfeae1b89
78422-001-21	73283c83-2cdf-48cb-a08c-328bfeae1b89
78422-001-22	73283c83-2cdf-48cb-a08c-328bfeae1b89
78422-001-23	73283c83-2cdf-48cb-a08c-328bfeae1b89
78422-001-24	73283c83-2cdf-48cb-a08c-328bfeae1b89
78422-001-25	73283c83-2cdf-48cb-a08c-328bfeae1b89
78422-001-26	73283c83-2cdf-48cb-a08c-328bfeae1b89
78422-001-27	73283c83-2cdf-48cb-a08c-328bfeae1b89
78422-001-28	73283c83-2cdf-48cb-a08c-328bfeae1b89

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
78422-001-01	MU instant hand sanitizer	10 mL in 1 BOTTLE, PLASTIC	GEL	10	1
78422-001-02	MU instant hand sanitizer	20 mL in 1 BOTTLE, PLASTIC	GEL	20	1
78422-001-03	MU instant hand sanitizer	30 mL in 1 BOTTLE, PLASTIC	GEL	30	1
78422-001-04	MU instant hand sanitizer	45 mL in 1 BOTTLE, PLASTIC	GEL	45	1
78422-001-05	MU instant hand sanitizer	50 mL in 1 BOTTLE, PLASTIC	GEL	50	1
78422-001-06	MU instant hand sanitizer	55 mL in 1 BOTTLE, PLASTIC	GEL	55	1
78422-001-07	MU instant hand sanitizer	60 mL in 1 BOTTLE, PLASTIC	GEL	60	1
78422-001-08	MU instant hand sanitizer	80 mL in 1 BOTTLE, PLASTIC	GEL	80	1
78422-001-09	MU instant hand sanitizer	100 mL in 1 BOTTLE, PLASTIC	GEL	100	1
78422-001-10	MU instant hand sanitizer	120 mL in 1 BOTTLE, PLASTIC	GEL	120	1
78422-001-11	MU instant hand sanitizer	180 mL in 1 BOTTLE, PLASTIC	GEL	180	1
78422-001-12	MU instant hand sanitizer	200 mL in 1 BOTTLE, PLASTIC	GEL	200	1
78422-001-13	MU instant hand sanitizer	237 mL in 1 BOTTLE, PLASTIC	GEL	237	1
78422-001-14	MU instant hand sanitizer	250 mL in 1 BOTTLE, PLASTIC	GEL	250	1
78422-001-15	MU instant hand sanitizer	300 mL in 1 BOTTLE, PLASTIC	GEL	300	1
78422-001-16	MU instant hand sanitizer	474 mL in 1 BOTTLE, PLASTIC	GEL	474	1
78422-001-17	MU instant hand sanitizer	500 mL in 1 BOTTLE, PLASTIC	GEL	500	1
78422-001-18	MU instant hand sanitizer	946 mL in 1 BOTTLE, PLASTIC	GEL	946	1
78422-001-19	MU instant hand sanitizer	1000 mL in 1 BOTTLE, PLASTIC	GEL	1000	1
78422-001-20	MU instant hand sanitizer	2000 mL in 1 BOTTLE, PLASTIC	GEL	2000	1
78422-001-21	MU instant hand sanitizer	3000 mL in 1 BOTTLE, PLASTIC	GEL	3000	1
78422-001-22	MU instant hand sanitizer	4000 mL in 1 BOTTLE, PLASTIC	GEL	4000	1
78422-001-23	MU instant hand sanitizer	5000 mL in 1 BOTTLE, PLASTIC	GEL	5000	1
78422-001-24	MU instant hand sanitizer	10000 mL in 1 BOTTLE, PLASTIC	GEL	10000	1
78422-001-25	MU instant hand sanitizer	20000 mL in 1 BOTTLE, PLASTIC	GEL	20000	1
78422-001-26	MU instant hand sanitizer	50000 mL in 1 BOTTLE, PLASTIC	GEL	50000	1
78422-001-27	MU instant hand sanitizer	100000 mL in 1 BOTTLE, PLASTIC	GEL	100000	1
78422-001-28	MU instant hand sanitizer	980 mL in 1 BOTTLE, PLASTIC	GEL	980	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
78422-001	MU INSTANT HAND SANITIZER (ALCOHOL) GEL [NINGBO ROYAL UNION CO., LTD.]	1	Legacy NDC, 28 package rows	20200610_73283c83-2cdf-48cb-a08c-328bfeae1b89.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
1305100	ethanol 75 % Topical Gel	PSN	73283c83-2cdf-48cb-a08c-328bfeae1b89	1
1305100	ethanol 0.75 ML/ML Topical Gel	SCD	73283c83-2cdf-48cb-a08c-328bfeae1b89	1
1305100	ethanol 75 % Topical Gel	SY	73283c83-2cdf-48cb-a08c-328bfeae1b89	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
78422-001-12	78422000112	200 mL in 1 BOTTLE, PLASTIC (78422-001-12)	200 ml	2020-05-20	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
MU instant hand sanitizer - Ningbo Royal Union Co., Ltd.	Ningbo Royal Union Co., Ltd.	2020-05-29	HUMAN OTC DRUG LABEL	1