Hand-Aid

Product NDC: 62257-122
11-digit product format: 622570122
Labeler code: 62257
Product ID: 62257-122_43f3f037-b359-8dfa-e063-6394a90aee39
Type: HUMAN OTC DRUG
Nonproprietary name: ALCOHOL
Dosage form: GEL
Route: TOPICAL
Labeler: ABC Compounding Co., Inc.
Application: M004
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2021-01-15
Substance: ALCOHOL
Active strength: .7 mL/mL
NDC exclude flag: No
Listing certified through: 2026-12-31
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 · 6 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Source date
excluded package	package	62257-122	62257-122-01	D	Discontinued by firm	2026-08-07
excluded package	package	62257-122	62257-122-21	D	Discontinued by firm	2026-08-07
excluded package	package	62257-122	62257-122-24	D	Discontinued by firm	2026-08-07
excluded package	package	62257-122	62257-122-28	D	Discontinued by firm	2026-08-07
excluded package	package	62257-122	62257-122-47	D	Discontinued by firm	2026-08-07
excluded package	package	62257-122	62257-122-55	D	Discontinued by firm	2026-08-07

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 · 16 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	62257-122-55	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	62257-122-21	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	62257-122-01	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	62257-122-28	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	62257-122-47	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	62257-122-24	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	62257-122-47	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	62257-122-24	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	62257-122-13	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	62257-122-21	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	62257-122-14	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	62257-122-01	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	62257-122-28	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	62257-122-55	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	62257-122-17	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

Additional Listing Data#

Finished product: Yes
Brand name base: Hand-Aid
Listing expiration: 2026-12-31

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 RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
581662	Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
Identifier	FDA.report destination
788d7584-bc33-49e8-90fd-767045ea2914	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
62257-122-01	Hand-Aid	1200 mL in 1 CARTRIDGE	GEL	1200	10
62257-122-13	Hand-Aid	800 mL in 1 BAG	GEL	800	10
62257-122-14	Hand-Aid	3785 mL in 1 BOTTLE, PLASTIC	GEL	3785	10
62257-122-17	Hand-Aid	532 mL in 1 BOTTLE, PLASTIC	GEL	532	10
62257-122-21	Hand-Aid	2.5 mL in 1 DOSE PACK	GEL	2.5	10
62257-122-24	Hand-Aid	118 mL in 1 BOTTLE, PLASTIC	GEL	118	10
62257-122-28	Hand-Aid	149 mL in 1 BOTTLE, PLASTIC	GEL	149	10
62257-122-47	Hand-Aid	473 mL in 1 BOTTLE, PLASTIC	GEL	473	10
62257-122-55	Hand-Aid	208200 mL in 1 DRUM	GEL	208200	10

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
62257-122	HAND-AID (ALCOHOL) GEL [ABC COMPOUNDING CO., INC.]	9	Current NDC, Legacy NDC, 9 package rows	20250425_788d7584-bc33-49e8-90fd-767045ea2914.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 · 424 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
TRIPLE ANTIBIOTIC	BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE	Vive Health LLC	236c62bf-3de0-0b3e-e063-6394a90ad6c6	2026-07-21	Warnings	Exact identifier application number: M004
TRIPLE ANTIBIOTIC	BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE	Vive Health LLC	21b38b00-1e64-83d8-e063-6294a90a07bd	2026-07-21	Warnings	Exact identifier application number: M004
DERMFREE Triple Antibiotic	TRIPLE ANTIBIOTIC	Jiangxi Yudexi Pharmaceutical Co., LTD	4a5a5603-3478-5f7a-e063-6294a90acc40	2026-07-21	Warnings	Exact identifier application number: M004
Bacitracin	BACITRACIN ZINC	Preferred Pharmaceuticals Inc.	e094566b-3b80-45ac-be73-54c798bbb763	2026-07-15	Warnings	Exact identifier application number: M004
Good Sense First Aid Antibiotic	BACITRACIN ZINC, NEOMYCIN, POLYMYXIN B	L. Perrigo Company	3eadd35c-3df2-4e46-b76d-a6e537895917	2026-07-10	Warnings	Exact identifier application number: M004
Ever Ready First Aid Triple Antibiotic	BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE	EVER READY FIRST AID	ee1ad6d7-e9c1-2b20-e053-2995a90a3366	2026-07-03	Warnings	Exact identifier application number: M004
Single Antibiotic with bacitracin	BACITRACIN ZINC	Safetec of America	4ae9a105-e3f9-4015-8844-085e0b34cdb6	2026-06-25	Warnings	Exact identifier application number: M004
Antibacterial Hand Wipes (0.13% Benzalkonium Chloride)	BENZALKONIUM CHLORIDE	Eleeo Brands LLC	551baf59-39b9-e994-e063-6294a90a65e6	2026-06-25	Warnings	Exact identifier application number: M004
Medi First Triple Antibiotic	BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE	Unifirst First Aid Corporation	545fa5b6-781c-18ae-e063-6294a90a2f0d	2026-06-16	Warnings	Exact identifier application number: M004
Triple Antibiotic	FIRST AID ANTIBIOTIC ORIGINAL STRENGTH	Aldermed Inc.	19eace87-b505-4be6-93b3-db5323e34216	2026-06-12	Warnings	Exact identifier application number: M004
Bacitracin	BACITRACIN	AlderMed Inc.	3f0eb4a0-f7bf-45f7-8885-92c65a4bd899	2026-06-08	Warnings	Exact identifier application number: M004
Bacitracin Zinc	FIRST AID ANTIBIOTIC	Aldermed Inc.	7f4bff4f-588d-4e45-8aa3-f95b4d746f25	2026-06-08	Warnings	Exact identifier application number: M004
Triple Antibiotic First Aid Antibiotic plus Pain Relief	BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, PRAMOXINE HCL	Aldermed Inc.	5bfc7776-1030-48ba-9df4-897c4984c9e6	2026-06-08	Warnings	Exact identifier application number: M004
Triple Antibiotic Plus Pain Relief	BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE	Sun Pharmaceutical Industries, Inc.	4545c043-8e8e-4288-b4d8-e6ec9d72f979	2026-06-04	Warnings	Exact identifier application number: M004
First Aid Kit, Orazen Inc	5 ADHESIVE BANDAGES, 2 ANTIBIOTIC OINTMENTS	Orazen Inc	525bcb89-af5b-8652-e063-6294a90a41a6	2026-06-03	Warnings	Exact identifier application number: M004
Triple Antibiotic	BACITRACIN ZINC, NEOMYCIN SULFATE, AND POLYMYXIN B SULFATE	Sun Pharmaceutical Industries, Inc.	d77239e6-5e81-439a-b0cd-f8be59169442	2026-06-02	Warnings	Exact identifier application number: M004
First Aid Antibiotic	BACITRACIN ZINC, NEOMYCIN, POLYMYXIN B	HyVee Inc	3ac9f0fc-e08c-49d9-9079-3ba0393c612b	2026-06-02	Warnings	Exact identifier application number: M004
Triple Antibiotic Plus Pain Relief	BACITRACIN, NEOMYCIN, POLYMYXIN B, PRAMOXINE HCL	HyVee Inc	69a4b642-b7ec-43cc-aa57-6858da0b3d63	2026-06-02	Warnings	Exact identifier application number: M004
Careland Triple Antibiotic	BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE	Planet (Anhui) Pharmaceutical Co., Ltd.	0e64179d-fce2-48fc-833e-ce43a54b987c	2026-05-31	Warnings	Exact identifier application number: M004
First Aid Antibiotic	BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE	Hubei Fanjian Medical Product Co.,Ltd	f44ab989-c618-1831-e053-2995a90adc8e	2026-05-28	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

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
581662	ethanol 70 % Topical Gel	PSN	788d7584-bc33-49e8-90fd-767045ea2914	10
581662	ethanol 0.7 ML/ML Topical Gel	SCD	788d7584-bc33-49e8-90fd-767045ea2914	10
581662	ethanol 70 % Topical Gel	SY	788d7584-bc33-49e8-90fd-767045ea2914	10
581662	ethyl alcohol 70 % Topical Gel	SY	788d7584-bc33-49e8-90fd-767045ea2914	10

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
62257-122-01	62257012201	1200 mL in 1 CARTRIDGE (62257-122-01)	1200 ml	2020-07-14	0000-00-00	No	No	Current
62257-122-13	62257012213	800 mL in 1 BAG (62257-122-13)	800 ml	2021-01-15	0000-00-00	No	No	Current
62257-122-14	62257012214	3785 mL in 1 BOTTLE, PLASTIC (62257-122-14)	3785 ml	2021-01-15	0000-00-00	No	No	Current
62257-122-17	62257012217	532 mL in 1 BOTTLE, PLASTIC (62257-122-17)	532 ml	2021-01-15	0000-00-00	No	No	Current
62257-122-21	62257012221	2.5 mL in 1 DOSE PACK (62257-122-21)	2.5 ml	2020-07-14	0000-00-00	No	No	Current
62257-122-24	62257012224	118 mL in 1 BOTTLE, PLASTIC (62257-122-24)	118 ml	2020-07-14	0000-00-00	No	No	Current
62257-122-28	62257012228	149 mL in 1 BOTTLE, PLASTIC (62257-122-28)	149 ml	2020-07-14	0000-00-00	No	No	Current
62257-122-47	62257012247	473 mL in 1 BOTTLE, PLASTIC (62257-122-47)	473 ml	2020-07-14	0000-00-00	No	No	Current
62257-122-55	62257012255	208200 mL in 1 DRUM (62257-122-55)	208200 ml	2020-07-14	0000-00-00	No	No	Current