Hand San

Product NDC: 59503-2605
11-digit product format: 595032605
Labeler code: 59503
Product ID: 59503-2605_51c86538-8a5c-6c84-e063-6294a90a42c2
Type: HUMAN OTC DRUG
Nonproprietary name: ALCOHOL
Dosage form: LIQUID
Route: TOPICAL
Labeler: Rochester Midland Corporation
Application: M004
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2021-03-11
Substance: ALCOHOL
Active strength: .7 mL/mL
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

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 · 5 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Source date
excluded package	package	59503-2605	59503-2605-1	D	Discontinued by firm	2026-10-16
excluded package	package	59503-2605	59503-2605-3	D	Discontinued by firm	2026-10-16
excluded package	package	59503-2605	59503-2605-4	D	Discontinued by firm	2026-10-16
excluded package	package	59503-2605	59503-2605-5	D	Discontinued by firm	2026-10-16
excluded package	package	59503-2605	59503-2605-6	D	Discontinued by firm	2026-10-16

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, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	59503-2605-3	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	59503-2605-5	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	59503-2605-4	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	59503-2605-1	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	59503-2605-6	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	59503-2605-8	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	59503-2605-3	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	59503-2605-6	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	59503-2605-2	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	59503-2605-8	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	59503-2605-1	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	59503-2605-7	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	59503-2605-5	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	59503-2605-4	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product: Yes
Brand name base: Hand San
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ALCOHOL	.7 mL/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
3K9958V90M	Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
2d89982d-d1fd-4a98-8b44-c2ae3545be58	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
59503-2605-1	Hand San	472 mL in 1 BOTTLE, PLASTIC	LIQUID	472	7
59503-2605-2	Hand San	3785 mL in 1 BOTTLE, PLASTIC	LIQUID	3785	7
59503-2605-3	Hand San	18900 mL in 1 CONTAINER	LIQUID	18900	7
59503-2605-4	Hand San	208200 mL in 1 DRUM	LIQUID	208200	7
59503-2605-5	Hand San	946 mL in 1 BOTTLE, PLASTIC	LIQUID	946	7
59503-2605-6	Hand San	2500 mL in 1 BOTTLE, PLASTIC	LIQUID	2500	7
59503-2605-7	Hand San	75600 mL in 1 DRUM	LIQUID	75600	7
59503-2605-8	Hand San	132500 mL in 1 DRUM	LIQUID	132500	7

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ALCOHOL	ACTIVE INGREDIENT	3K9958V90M	HAND SAN (ALCOHOL) LIQUID [ROCHESTER MIDLAND CORPORATION]	1
ALCOHOL	ACTIVE MOIETY	3K9958V90M	HAND SAN (ALCOHOL) LIQUID [ROCHESTER MIDLAND CORPORATION]	1
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	HAND SAN (ALCOHOL) LIQUID [ROCHESTER MIDLAND CORPORATION]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	HAND SAN (ALCOHOL) LIQUID [ROCHESTER MIDLAND CORPORATION]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
59503-2605	HAND SAN (ALCOHOL) LIQUID [ROCHESTER MIDLAND CORPORATION]	5	Current NDC, Legacy NDC, 8 package rows	20250112_2d89982d-d1fd-4a98-8b44-c2ae3545be58.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 8 of 22 · 424 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
GASCO ANTIBACTERIAL	BENZALKONIUM CHLORIDE	GASCO INDUSTRIAL CORP	411ffefe-16e5-a2e0-e063-6394a90a0cd4	2025-10-14	Warnings	Exact identifier application number: M004
Triple Antibiotic	BACITRACIN ZINC, NEOMYCIN SULFATE , POLYMYXIN B SULFATE.	TRIFECTA PHARMACEUTICALS USA LLC	4124e9e2-397f-8921-e063-6394a90a5ffe	2025-10-14	Warnings	Exact identifier application number: M004
Antibiotic	NEOMYCIN SULFATE	Total Resources International	0725364b-b243-4891-af2f-a6049366d038	2025-10-10	Warnings	Exact identifier application number: M004
MediChoice Bacitracin	BACITRACIN	O&M HALYARD, INC.	78079b94-c6fc-4529-aaad-8186924ecba5	2025-10-09	Warnings	Exact identifier application number: M004
MediChoice Triple Antibiotic	BACITRACIN	O&M HALYARD, INC.	8369f399-6f64-4441-be72-1f16c7306c0a	2025-10-09	Warnings	Exact identifier application number: M004
Triple Antibiotic	BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE	Medline Industries, LP	301ebb9a-033b-4f04-99ff-571e921924ca	2025-10-09	Warnings	Exact identifier application number: M004
First Aid Antibiotic	BACITRACIN ZINC	Medline Industries, LP	f8282204-f9b9-486f-b18b-dc5ba85cce10	2025-10-09	Warnings	Exact identifier application number: M004
TheraCare Triple Antibiotic Pain Relief	BACITRACIN,NEOMYCIN,POLYMXIN, PRAMOXINE	Veridian Healthcare	faf73908-324f-27f5-e053-6394a90aa06e	2025-10-02	Warnings	Exact identifier application number: M004
Viaderma Care First Aid	BACITRACIN ZINC	ViaDerma Distribution, Inc.	dabb7ce8-3284-4dfc-bc6e-38a691be43c1	2025-10-02	Warnings	Exact identifier application number: M004
Double Antibiotic	BACITRACIN ZINC POLYMYXIN B SULFATE	Encube Ethicals, Inc.	8f00b059-6729-4fae-8e8c-e14fe8838c59	2025-09-30	Warnings	Exact identifier application number: M004
Xpect Triple Antibiotic	BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE	Cintas Corporation	39355db3-24d7-485f-9ce0-f0e466e96593	2025-09-26	Warnings	Exact identifier application number: M004
TRIPLE ANTIBIOTIC	BACITRACIN ZINC NEOMYCIN SULFATE POLYMYXIN B SULFATE PRAMOXINE HCL	Encube Ethicals, Inc.	dfea6b2e-cd76-439d-a3da-64e2d8717163	2025-09-25	Warnings	Exact identifier application number: M004
TRIPLE ANTIBIOTIC	BACITRACIN ZINC NEOMYCIN SULFATE POLYMYXIN B SULFATE	Encube Ethicals, Inc.	2e985ad0-aa50-4c6b-b0af-1d61489a9fda	2025-09-25	Warnings	Exact identifier application number: M004
Medi-First Triple Antibiotic	BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE	Unifirst First Aid Corporation	f2f0a1da-3e33-3c1a-e053-2a95a90a12b1	2025-09-09	Warnings	Exact identifier application number: M004
Ecolab Triple Antibiotic	BACITRACIN, NEOMYCIN SULFATE, POLYMYXIN B SULFATE	Ecolabs Food Safety Specialties, Inc.	4aef8f98-db76-07f2-e054-00144ff8d46c	2025-09-09	Warnings	Exact identifier application number: M004
Triple Antibiotic	BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE	Unifirst First Aid Corporation	d265f094-e654-4c68-9215-b5d061af885d	2025-09-08	Warnings	Exact identifier application number: M004
Triple Antibiotic	BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE	Unifirst First Aid Corporation	d7c1a10e-c38d-4ae8-9a27-c07c2208ca84	2025-09-08	Warnings	Exact identifier application number: M004
Thompson Triple Antibiotic	BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE	Thompson	f883c4cb-c32c-76e3-e053-6294a90aa4fc	2025-09-08	Warnings	Exact identifier application number: M004
Thompson Triple Antibiotic	BACITRACIN ZINC, POLYMYXIN B SULFATE, NEOMYCIN SULFATE	Thompson	de9489de-e677-2bd3-e053-2a95a90acfb4	2025-09-08	Warnings	Exact identifier application number: M004
BACITRACIN ZINC	FIRST AID ANTIBIOTIC	Encube Ethicals, Inc.	613cbed4-9790-4e6b-a61b-b7b7a8ee59c9	2025-09-04	Warnings	Exact identifier application number: M004

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
3K9958V90M	ALCOHOL	64-17-5	ALCOHOL

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
59503-2605-1	59503260501	472 mL in 1 BOTTLE, PLASTIC (59503-2605-1)	472 ml	2021-03-11	0000-00-00	No	No	Current
59503-2605-2	59503260502	3785 mL in 1 BOTTLE, PLASTIC (59503-2605-2)	3785 ml	2021-03-11	0000-00-00	No	No	Current
59503-2605-3	59503260503	18900 mL in 1 CONTAINER (59503-2605-3)	18900 ml	2021-03-11	0000-00-00	No	No	Current
59503-2605-4	59503260504	208200 mL in 1 DRUM (59503-2605-4)	208200 ml	2021-03-11	0000-00-00	No	No	Current
59503-2605-5	59503260505	946 mL in 1 BOTTLE, PLASTIC (59503-2605-5)	946 ml	2021-03-11	0000-00-00	No	No	Current
59503-2605-6	59503260506	2500 mL in 1 BOTTLE, PLASTIC (59503-2605-6)	2500 ml	2021-03-11	0000-00-00	No	No	Current
59503-2605-7	59503260507	75600 mL in 1 DRUM (59503-2605-7)	75600 ml	2021-03-11	0000-00-00	No	No	Current
59503-2605-8	59503260508	132500 mL in 1 DRUM (59503-2605-8)	132500 ml	2021-03-11	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Hand San 6150 Drug Facts and Label	Rochester Midland Corporation \| ABC Compounding Co., Inc.	2026-05-14	HUMAN OTC DRUG LABEL	7