anti-bacterial hand sanitizer

Product NDC: 53603-1018
Requested package NDC: 53603-1018-1
11-digit product format: 536031018
Labeler code: 53603
Product ID: 53603-1018_130c2c15-7fc5-4eff-e054-00144ff8d46c
Type: HUMAN OTC DRUG
Nonproprietary name: ETHYL ALCOHOL
Dosage form: GEL
Route: TOPICAL
Labeler: BB17, LLC
Application: part333E
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2015-04-06
Marketing end: 0000-00-00
Substance: ALCOHOL
Active strength: 62 mL/100mL
NDC exclude flag: No
Listing certified through: 2020-12-31
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	53603-1018	53603-1018-1	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 · 15 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…`

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
7792dadb-52b6-46b6-8fdf-80b1171065b5	Product name	1	20180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
53603-1018-1	2023-01-30	C162847	48780-1	f386c649-d193-0266-e053-dadaa90a7c1a	130c2c15-7fc4-4eff-e054-00144ff8d46c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
53603-1018-1	anti-bacterial hand sanitizer	29.5 mL in 1 BOTTLE, SPRAY	GEL	29.5		1

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ALCOHOL	ACTIVE INGREDIENT	3K9958V90M	ANTI-BACTERIAL HAND SANITIZER (ETHYL ALCOHOL) GEL [BB17, LLC]	1
ALCOHOL	ACTIVE MOIETY	3K9958V90M	ANTI-BACTERIAL HAND SANITIZER (ETHYL ALCOHOL) GEL [BB17, LLC]	1
.ALPHA.-TOCOPHEROL ACETATE	INACTIVE INGREDIENT	9E8X80D2L0	ANTI-BACTERIAL HAND SANITIZER (ETHYL ALCOHOL) GEL [BB17, LLC]	1
ALOE VERA LEAF	INACTIVE INGREDIENT	ZY81Z83H0X	ANTI-BACTERIAL HAND SANITIZER (ETHYL ALCOHOL) GEL [BB17, LLC]	1
CARBOMER INTERPOLYMER TYPE A (55000 CPS)	INACTIVE INGREDIENT	59TL3WG5CO	ANTI-BACTERIAL HAND SANITIZER (ETHYL ALCOHOL) GEL [BB17, LLC]	1
FD&C YELLOW NO. 5	INACTIVE INGREDIENT	I753WB2F1M	ANTI-BACTERIAL HAND SANITIZER (ETHYL ALCOHOL) GEL [BB17, LLC]	1
GLYCERIN	INACTIVE INGREDIENT	PDC6A3C0OX	ANTI-BACTERIAL HAND SANITIZER (ETHYL ALCOHOL) GEL [BB17, LLC]	1
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	ANTI-BACTERIAL HAND SANITIZER (ETHYL ALCOHOL) GEL [BB17, LLC]	1
TROLAMINE	INACTIVE INGREDIENT	9O3K93S3TK	ANTI-BACTERIAL HAND SANITIZER (ETHYL ALCOHOL) GEL [BB17, LLC]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	ANTI-BACTERIAL HAND SANITIZER (ETHYL ALCOHOL) GEL [BB17, LLC]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
53603-1018	ANTI-BACTERIAL HAND SANITIZER (ETHYL ALCOHOL) GEL [BB17, LLC]	1	Legacy NDC, 1 package rows	20150421_130c2c15-7fc4-4eff-e054-00144ff8d46c.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
581660	ethanol 62 % Topical Gel	PSN	130c2c15-7fc4-4eff-e054-00144ff8d46c	1
581660	ethanol 0.62 ML/ML Topical Gel	SCD	130c2c15-7fc4-4eff-e054-00144ff8d46c	1
581660	ethanol 62 % Topical Gel	SY	130c2c15-7fc4-4eff-e054-00144ff8d46c	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
53603-1018-1	53603101801	29.5 mL in 1 BOTTLE, SPRAY (53603-1018-1)	29.5 ml	2015-04-06	0000-00-00	No	No	Current