Hand Sanitizer

Product NDC: 75814-102
Requested package NDC: 75814-102-08
11-digit product format: 758140102
Labeler code: 75814
Product ID: 75814-102_67efe5f7-31a6-4a84-84a5-66d4df4fe2af
Type: HUMAN OTC DRUG
Nonproprietary name: ISOPROPYL ALCOHOL, COPPER, SILVER, POTASSIUM ALUM, and CAMPHOR oil, WHITE
Dosage form: GEL
Route: TOPICAL
Labeler: SERENITY TECHNOLOGIES INC.
Marketing category: UNAPPROVED DRUG OTHER
Marketing start: 2020-04-27
Marketing end: 0000-00-00
Substance: ISOPROPYL ALCOHOL; COPPER; SILVER; POTASSIUM ALUM; CAMPHOR OIL, WHITE
Active strength: 750 mL/1000mL; mg/1000mL; mg/1000mL; mg/1000mL; g/1000mL
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	75814-102	75814-102-08	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
c599c4a0-705d-4ebb-ab1f-977af038f96a	Product name	1	20251124

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
75814-102-01	2022-01-28	C162847	48780-1	d6a99b39-d925-a426-e053-dadaa90af4c2	Hand Sanitizer
75814-102-02	2022-01-28	C162847	48780-1	d6a99b39-d925-a426-e053-dadaa90af4c2	Hand Sanitizer
75814-102-08	2022-01-28	C162847	48780-1	d6a99b39-d925-a426-e053-dadaa90af4c2	Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
75814-102-01	Hand Sanitizer	29.6 mL in 1 BOTTLE	GEL	29.6	1
75814-102-02	Hand Sanitizer	59.1 mL in 1 BOTTLE	GEL	59.1	1
75814-102-08	Hand Sanitizer	236.6 mL in 1 BOTTLE	GEL	236.6	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
75814-102	HAND SANITIZER (ISOPROPYL ALCOHOL, COPPER, SILVER, POTASSIUM ALUM, AND CAMPHOR OIL, WHITE) GEL [SERENITY TECHNOLOGIES INC.]	1	Legacy NDC, 3 package rows	20200506_a29e0f18-0e48-4fce-b479-125a6ff84533.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
ND2M416302	ISOPROPYL ALCOHOL	67-63-0	ISOPROPYL ALCOHOL
789U1901C5	COPPER	7440-50-8	COPPER
3M4G523W1G	SILVER	7440-22-4	SILVER
1L24V9R23S	POTASSIUM ALUM	7784-24-9	POTASSIUM ALUM
26P3H26Z9X	CAMPHOR OIL, WHITE		CAMPHOR OIL, WHITE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
75814-102-08	75814010208	236.6 mL in 1 BOTTLE (75814-102-08)	236.6 ml	2020-04-27	0000-00-00	No	No	Current