Antibacterial hand sanitizer

Product NDC: 78887-001
Requested package NDC: 78887-001-01
11-digit product format: 788870001
Labeler code: 78887
Product ID: 78887-001_5057eaa2-8fca-4644-b35b-4831aa48d588
Type: HUMAN OTC DRUG
Nonproprietary name: Alcohol
Dosage form: LIQUID
Route: TOPICAL
Labeler: Ankit LLC
Application: part333A
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2020-06-13
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	78887-001	78887-001-01	I	Inactivated by FDA		2026-10-12

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
78887-001-01	39f3126d-475c-41a3-84ae-110201249df5
78887-001-02	39f3126d-475c-41a3-84ae-110201249df5
78887-001-03	39f3126d-475c-41a3-84ae-110201249df5
78887-001-04	39f3126d-475c-41a3-84ae-110201249df5
78887-001-05	39f3126d-475c-41a3-84ae-110201249df5
78887-001-06	39f3126d-475c-41a3-84ae-110201249df5
78887-001-07	39f3126d-475c-41a3-84ae-110201249df5
78887-001-08	39f3126d-475c-41a3-84ae-110201249df5
78887-001-09	39f3126d-475c-41a3-84ae-110201249df5
78887-001-10	39f3126d-475c-41a3-84ae-110201249df5
78887-001-11	39f3126d-475c-41a3-84ae-110201249df5
78887-001-12	39f3126d-475c-41a3-84ae-110201249df5
78887-001-13	39f3126d-475c-41a3-84ae-110201249df5
78887-001-14	39f3126d-475c-41a3-84ae-110201249df5
78887-001-15	39f3126d-475c-41a3-84ae-110201249df5
78887-001-16	39f3126d-475c-41a3-84ae-110201249df5
78887-001-17	39f3126d-475c-41a3-84ae-110201249df5
78887-001-18	39f3126d-475c-41a3-84ae-110201249df5
78887-001-19	39f3126d-475c-41a3-84ae-110201249df5
78887-001-20	39f3126d-475c-41a3-84ae-110201249df5
78887-001-21	39f3126d-475c-41a3-84ae-110201249df5
78887-001-22	39f3126d-475c-41a3-84ae-110201249df5
78887-001-23	39f3126d-475c-41a3-84ae-110201249df5
78887-001-24	39f3126d-475c-41a3-84ae-110201249df5
78887-001-25	39f3126d-475c-41a3-84ae-110201249df5
78887-001-26	39f3126d-475c-41a3-84ae-110201249df5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
78887-001-01	Antibacterial hand sanitizer	29 mL in 1 BOTTLE, PLASTIC	LIQUID	29	1
78887-001-02	Antibacterial hand sanitizer	59 mL in 1 BOTTLE, PLASTIC	LIQUID	59	1
78887-001-03	Antibacterial hand sanitizer	100 mL in 1 BOTTLE, PLASTIC	LIQUID	100	1
78887-001-04	Antibacterial hand sanitizer	118 mL in 1 BOTTLE, PLASTIC	LIQUID	118	1
78887-001-05	Antibacterial hand sanitizer	237 mL in 1 BOTTLE, PLASTIC	LIQUID	237	1
78887-001-06	Antibacterial hand sanitizer	250 mL in 1 BOTTLE, PLASTIC	LIQUID	250	1
78887-001-07	Antibacterial hand sanitizer	473 mL in 1 BOTTLE, PLASTIC	LIQUID	473	1
78887-001-08	Antibacterial hand sanitizer	500 mL in 1 BOTTLE, PLASTIC	LIQUID	500	1
78887-001-09	Antibacterial hand sanitizer	887 mL in 1 BOTTLE, PLASTIC	LIQUID	887	1
78887-001-10	Antibacterial hand sanitizer	946 mL in 1 BOTTLE, PLASTIC	LIQUID	946	1
78887-001-11	Antibacterial hand sanitizer	1000 mL in 1 BOTTLE, PLASTIC	LIQUID	1000	1
78887-001-12	Antibacterial hand sanitizer	2000 mL in 1 BOTTLE, PLASTIC	LIQUID	2000	1
78887-001-13	Antibacterial hand sanitizer	3000 mL in 1 BOTTLE, PLASTIC	LIQUID	3000	1
78887-001-14	Antibacterial hand sanitizer	3800 mL in 1 BOTTLE, PLASTIC	LIQUID	3800	1
78887-001-15	Antibacterial hand sanitizer	4000 mL in 1 BOTTLE, PLASTIC	LIQUID	4000	1
78887-001-16	Antibacterial hand sanitizer	5000 mL in 1 BOTTLE, PLASTIC	LIQUID	5000	1
78887-001-17	Antibacterial hand sanitizer	7600 mL in 1 BOTTLE, PLASTIC	LIQUID	7600	1
78887-001-18	Antibacterial hand sanitizer	10000 mL in 1 BOTTLE, PLASTIC	LIQUID	10000	1
78887-001-19	Antibacterial hand sanitizer	11400 mL in 1 BOTTLE, PLASTIC	LIQUID	11400	1
78887-001-20	Antibacterial hand sanitizer	18900 mL in 1 BOTTLE, PLASTIC	LIQUID	18900	1
78887-001-21	Antibacterial hand sanitizer	20000 mL in 1 BOTTLE, PLASTIC	LIQUID	20000	1
78887-001-22	Antibacterial hand sanitizer	37900 mL in 1 BOTTLE, PLASTIC	LIQUID	37900	1
78887-001-23	Antibacterial hand sanitizer	50000 mL in 1 BOTTLE, PLASTIC	LIQUID	50000	1
78887-001-24	Antibacterial hand sanitizer	100000 mL in 1 BOTTLE, PLASTIC	LIQUID	100000	1
78887-001-25	Antibacterial hand sanitizer	150000 mL in 1 BOTTLE, PLASTIC	LIQUID	150000	1
78887-001-26	Antibacterial hand sanitizer	200000 mL in 1 BOTTLE, PLASTIC	LIQUID	200000	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
78887-001	ANTIBACTERIAL HAND SANITIZER (ALCOHOL) LIQUID [ANKIT LLC]	1	Legacy NDC, 26 package rows	20200616_39f3126d-475c-41a3-84ae-110201249df5.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	39f3126d-475c-41a3-84ae-110201249df5	1
1047755	ethanol 0.75 ML/ML Topical Solution	SCD	39f3126d-475c-41a3-84ae-110201249df5	1
1047755	ethanol 75 % Topical Solution	SY	39f3126d-475c-41a3-84ae-110201249df5	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
78887-001-01	78887000101	29 mL in 1 BOTTLE, PLASTIC (78887-001-01)	29 ml	2020-06-13	0000-00-00	No	No	Current