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	2026-10-02
excluded package	package	59503-2605	59503-2605-3	D	Discontinued by firm	2026-10-02
excluded package	package	59503-2605	59503-2605-4	D	Discontinued by firm	2026-10-02
excluded package	package	59503-2605	59503-2605-5	D	Discontinued by firm	2026-10-02
excluded package	package	59503-2605	59503-2605-6	D	Discontinued by firm	2026-10-02

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 1 of 22 · 434 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Triple Antibiotic	BACITRACIN ZINC, NEOMYCIN SULFATE, AND POLYMYXIN B SULFATE	NuCare Pharmaceutical, Inc.	5b14499e-e45c-7c05-e063-6294a90a1cc2	2026-09-09	Warnings	Exact identifier application number: M004
American Safety and First Aid Triple Antibiotic	BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE	Orazen Inc	eb0df2da-1688-c477-e053-2995a90a74a2	2026-09-07	Warnings	Exact identifier application number: M004
American Safety and First Aid Triple Antibiotic	BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE	Orazen Inc	eb0d108f-42bf-3364-e053-2a95a90a4542	2026-09-07	Warnings	Exact identifier application number: M004
MEDI-FIRST	BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE	Orazen Inc	f4e4d0a4-b90c-99b0-e053-2995a90ab423	2026-09-04	Warnings	Exact identifier application number: M004
Lil Drug Store Triple Antibiotic	BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE	ORAZEN INC	e6e5263b-328f-4775-9fac-34302f050ce0	2026-09-04	Warnings	Exact identifier application number: M004
MEDI-FIRST	BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE	Orazen Inc	f4e42c5c-e080-4efb-e053-2a95a90af52e	2026-09-04	Warnings	Exact identifier application number: M004
MEDI-FIRST	BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE	Orazen Inc	f4e4854a-ee01-df72-e053-2995a90aa8ea	2026-09-04	Warnings	Exact identifier application number: M004
Circle K Triple Antibiotic	BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE	ORAZEN INC	84c3f7e4-b28b-40bb-8d9d-7c8d679e3a3a	2026-09-04	Warnings	Exact identifier application number: M004
First Aid Antibiotic	BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B, PRAMOXINE HCL	Walgreen Company	b982091a-5aa0-4bbc-bb1d-08016f6d0a70	2026-09-03	Warnings	Exact identifier application number: M004
SurviveX Triple Antibiotic	TRIPLE ANTIBIOTIC	Nantong Health & Beyond Hygienic Products Inc.	5a7cb52d-a60c-b947-e063-6394a90afb0d	2026-09-02	Warnings	Exact identifier application number: M004
triple antibiotic	BACITRACIN ZINC, NEOMYCIN, POLYMYXIN B	Walgreen Company	4f3cfe39-2df8-48b4-954d-5997217c92ba	2026-08-31	Warnings	Exact identifier application number: M004
First Aid Antibiotic	BACITRACIN ZINC	NINGBO TIANBO FIRST AID PRODUCT CO., LTD.	217aa2b8-94f5-468a-99b4-52824a77b573	2026-08-28	Warnings	Exact identifier application number: M004
OP Triple Antibiotic	BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE	Yiwu Ori-Power Medtech Co., Ltd.	03f3cce9-7e9f-90a6-e063-6294a90a660b	2026-08-28	Warnings	Exact identifier application number: M004
Alcare Extra Hand Sanitizer	ALCOHOL	SC Johnson Professional USA Inc.	5dc007a2-61fa-4115-a82c-1aa489a6bd39	2026-08-27	Warnings	Exact identifier application number: M004
InstantFoam Complete PURE	ALCOHOL	SC Johnson Professional USA Inc.	398ca23c-7202-4670-be14-9829675f7174	2026-08-27	Warnings	Exact identifier application number: M004
Be Smart Get Prepared Triple Antibiotic	BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE	Total Resources International, Inc	57ed1a03-7e1b-4eb4-8001-dfd118805edc	2026-08-24	Warnings	Exact identifier application number: M004
Claravie	BACITRACIN ZINC	Gentell LLC	59c5a363-6d79-d07e-e063-6294a90a8753	2026-08-24	Warnings	Exact identifier application number: M004
Claravie	BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B	Gentell LLC	597cb2f0-ff05-a1ab-e063-6294a90acda9	2026-08-20	Warnings	Exact identifier application number: M004
Medpride First Aid	BACITRACIN ZINC NEOMYCIN SULFATE POLYMYXIN B SULFATE	Shield Line LLC	5ba3e703-7873-4724-a0bf-bb22d8a25748	2026-08-18	Warnings	Exact identifier application number: M004
Medpride First Aid	BACITRACIN ZINC	Shield Line LLC	e6a6fb0f-5ab7-4647-84a0-7b9948eed303	2026-08-18	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