Hand Sanitizer

Product NDC: 76844-101
Requested package NDC: 76844-101-04
11-digit product format: 768440101
Labeler code: 76844
Product ID: 76844-101_a4e584c1-d9c6-cdf1-e053-2995a90a06dc
Type: HUMAN OTC DRUG
Nonproprietary name: ALCOHOL
Dosage form: LIQUID
Route: TOPICAL
Labeler: Guangzhou Jieyi Daily Chemical Products Co., Ltd.
Application: part333A
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2020-03-30
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	76844-101	76844-101-04	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 · 19 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…`
2021-12-27 23:28 UTC · source 2021-12-27	`8dfbde2a14a4…`	`c9ff85d89658…`

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
76844-101-01	Hand Sanitizer
76844-101-02	Hand Sanitizer
76844-101-03	Hand Sanitizer
76844-101-04	Hand Sanitizer
76844-101-05	Hand Sanitizer
76844-101-06	Hand Sanitizer
76844-101-07	Hand Sanitizer
76844-101-08	Hand Sanitizer
76844-101-09	Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
76844-101-01	Hand Sanitizer	30 mL in 1 BOTTLE	LIQUID	30	2
76844-101-02	Hand Sanitizer	60 mL in 1 BOTTLE	LIQUID	60	2
76844-101-03	Hand Sanitizer	100 mL in 1 BOTTLE	LIQUID	100	2
76844-101-04	Hand Sanitizer	300 mL in 1 BOTTLE	LIQUID	300	2
76844-101-05	Hand Sanitizer	500 mL in 1 BOTTLE	LIQUID	500	2
76844-101-06	Hand Sanitizer	1000 mL in 1 BOTTLE	LIQUID	1000	2
76844-101-07	Hand Sanitizer	15 mL in 1 BOTTLE	LIQUID	15	2
76844-101-08	Hand Sanitizer	237 mL in 1 BOTTLE	LIQUID	237	2
76844-101-09	Hand Sanitizer	3000 mL in 1 BOTTLE	LIQUID	3000	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
76844-101	HAND SANITIZER (ALCOHOL) LIQUID [GUANGZHOU JIEYI DAILY CHEMICAL PRODUCTS CO., LTD.]	2	Legacy NDC, 9 package rows	20200506_a43c324c-cc1c-025d-e053-2995a90ac9c3.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
1047755	ethanol 75 % Topical Solution	PSN	a43c324c-cc1c-025d-e053-2995a90ac9c3	2
1047755	ethanol 0.75 ML/ML Topical Solution	SCD	a43c324c-cc1c-025d-e053-2995a90ac9c3	2
1047755	ethanol 75 % Topical Solution	SY	a43c324c-cc1c-025d-e053-2995a90ac9c3	2

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
76844-101-04	76844010104	300 mL in 1 BOTTLE (76844-101-04)	300 ml	2020-03-30	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Hand Sanitizer	Guangzhou Jieyi Daily Chemical Products Co., Ltd.	2020-05-05	HUMAN OTC DRUG LABEL	2