Alcohol

Product NDC: 30142-809
11-digit product format: 301420809
Labeler code: 30142
Product ID: 30142-809_5a825615-4303-cef5-e063-6294a90ab61f
Type: HUMAN OTC DRUG
Nonproprietary name: Isopropyl Alcohol
Dosage form: SWAB
Route: TOPICAL
Labeler: The Kroger Company
Application: M003
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2010-03-31
Substance: ISOPROPYL ALCOHOL
Active strength: 70 mL/100mL
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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	30142-809		I	Inactivated by FDA		2026-10-23
excluded package	package	30142-809	30142-809-09	I	Inactivated by FDA		2026-10-23

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 · 47 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 product	product		I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	30142-809-09	I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	30142-809-09	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	30142-809-09	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	30142-809-09	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	30142-809-09	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	30142-809-09	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		I	Inactivated by FDA	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	30142-809-09	I	Inactivated by FDA	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		I	Inactivated by FDA	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	30142-809-09	I	Inactivated by FDA	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		I	Inactivated by FDA	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	30142-809-09	I	Inactivated by FDA	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		I	Inactivated by FDA	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	30142-809-09	I	Inactivated by FDA	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		I	Inactivated by FDA	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	30142-809-09	I	Inactivated by FDA	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		I	Inactivated by FDA	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	30142-809-09	I	Inactivated by FDA	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded product	product		I	Inactivated by FDA	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded package	package	30142-809-09	I	Inactivated by FDA	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded product	product		I	Inactivated by FDA	`834df4deac94…`	`adcc014656a3…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	30142-809-09	I	Inactivated by FDA	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded product	product		I	Inactivated by FDA	`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	30142-809-09	I	Inactivated by FDA	`1332a3947898…`	`d4bfe170f9cd…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded product	product		I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	30142-809-09	I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded product	product		I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	30142-809-09	I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded product	product		I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	30142-809-09	I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded product	product		I	Inactivated by FDA	`8dfbde2a14a4…`	`c9ff85d89658…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded package	package	30142-809-09	I	Inactivated by FDA	`8dfbde2a14a4…`	`c9ff85d89658…`
2020-12-18 03:04 UTC · source 2020-12-17	excluded product	product		I	Inactivated by FDA	`e2bbac7714bc…`	`27bdfed8d636…`
2020-12-18 03:04 UTC · source 2020-12-17	excluded package	package	30142-809-09	I	Inactivated by FDA	`e2bbac7714bc…`	`27bdfed8d636…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded product	product		I	Inactivated by FDA	`9bebd1f3094a…`	`5416666fcb17…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded package	package	30142-809-09	I	Inactivated by FDA	`9bebd1f3094a…`	`5416666fcb17…`
2019-12-08 06:16 UTC · source 2019-12-05	excluded product	product		E	Excluded after deficient or non-compliant submission was not corrected	`110d247fa046…`	`a55b01930146…`
2019-12-08 06:16 UTC · source 2019-12-05	excluded product	product		E	Excluded after deficient or non-compliant submission was not corrected	`110d247fa046…`	`a55b01930146…`
2019-12-08 06:16 UTC · source 2019-12-05	excluded package	package	30142-809-31	E	Excluded after deficient or non-compliant submission was not corrected	`110d247fa046…`	`a55b01930146…`
2019-12-08 06:16 UTC · source 2019-12-05	excluded package	package	30142-809-30	E	Excluded after deficient or non-compliant submission was not corrected	`110d247fa046…`	`a55b01930146…`
2019-12-08 06:16 UTC · source 2019-12-05	excluded package	package	30142-809-09	E	Excluded after deficient or non-compliant submission was not corrected	`110d247fa046…`	`a55b01930146…`

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: Alcohol
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ISOPROPYL ALCOHOL	70 mL/100mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
ND2M416302	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
797544	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
6551187f-5cde-4149-931f-b057bd760750	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1	Product name	1	20230829

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Indexing SPL table
NDC	Effective	Indexing SPL	Related label
30142-809-30	2020-04-22	9d75b9d0-7621-f424-e053-dadaa90a57ce	30142-809 Kroger Alcohol Prep Pads
30142-809-30	2020-04-22	9d75b9d0-7621-f424-e053-dadaa90a57ce	30142-809 Kroger Alcohol Prep Pads
30142-809-31	2020-04-22	9d75b9d0-7621-f424-e053-dadaa90a57ce	30142-809 Kroger Alcohol Prep Pads
30142-809-31	2020-04-22	9d75b9d0-7621-f424-e053-dadaa90a57ce	30142-809 Kroger Alcohol Prep Pads
30142-809-09	2020-01-31	9d75b9d0-5cd1-f424-e053-dadaa90a57ce	Drug Facts
30142-809-30	2020-01-31	9d75b9d0-7621-f424-e053-dadaa90a57ce	30142-809 Kroger Alcohol Prep Pads
30142-809-30	2020-01-31	9d75b9d0-7621-f424-e053-dadaa90a57ce	30142-809 Kroger Alcohol Prep Pads
30142-809-31	2020-01-31	9d75b9d0-7621-f424-e053-dadaa90a57ce	30142-809 Kroger Alcohol Prep Pads
30142-809-31	2020-01-31	9d75b9d0-7621-f424-e053-dadaa90a57ce	30142-809 Kroger Alcohol Prep Pads

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
30142-809-30	Alcohol	100 in 1 BOX	SWAB	100	11
30142-809-30	Alcohol	1 in 1 PACKET	SWAB	1	11
30142-809-31	Alcohol	1 in 1 PACKET	SWAB	1	11
30142-809-31	Alcohol	140 in 1 BOX	SWAB	140	11
30142-809-09	Isopropyl Alcohol	100 in 1 BOX	SWAB	100	1

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ISOPROPYL ALCOHOL	ACTIVE INGREDIENT	ND2M416302	ALCOHOL (ISOPROPYL ALCOHOL) SWAB [THE KROGER COMPANY]	5
ISOPROPYL ALCOHOL	ACTIVE MOIETY	ND2M416302	ALCOHOL (ISOPROPYL ALCOHOL) SWAB [THE KROGER COMPANY]	5
WATER	INACTIVE INGREDIENT	059QF0KO0R	ALCOHOL (ISOPROPYL ALCOHOL) SWAB [THE KROGER COMPANY]	5
Isopropyl Alcohol	ACTIVE INGREDIENT	ND2M416302	ISOPROPYL ALCOHOL SWAB [THE KROGER COMPANY]	1
Isopropyl Alcohol	ACTIVE MOIETY	ND2M416302	ISOPROPYL ALCOHOL SWAB [THE KROGER COMPANY]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
30142-809	ALCOHOL (ISOPROPYL ALCOHOL) SWAB [THE KROGER COMPANY]	11	Current NDC, Legacy NDC, 4 package rows	20250105_6551187f-5cde-4149-931f-b057bd760750.zip
30142-809	ISOPROPYL ALCOHOL SWAB [THE KROGER COMPANY]	1	Current NDC, Legacy NDC, 1 package rows	20100406_4eca7228-4bfc-4b6c-839e-73b02faa4d54.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 81 of 114 · 2,277 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Unguentine	PHENOL, ZINC OXIDE	Oakhurst Company	327038a1-b825-1199-e063-6394a90a7f5f	2025-04-10	Warnings	Exact identifier application number: M003
Northside Hospital Grey Amenity Kit	SODIUM MONOFLUOROPHOSPATE	ASP Global, LLC	a3cc89df-be1b-4d9a-8ba3-857885325422	2025-04-09	Warnings	Exact identifier application number: M003
Isopropyl alcohol 70 percent	ISOPROPYL ALCOHOL	TOP CARE (Topco Associates LLC)	afe23634-27a4-46cf-b428-8fa3a274712c	2025-04-09	Warnings	Exact identifier application number: M003
Isopropyl Alcohol 91 percent	ISOPROPYL ALCOHOL	TOP CARE (Topco Associates LLC)	3c70ba1c-b12f-4a98-b993-1179ebe3e070	2025-04-09	Warnings	Exact identifier application number: M003
Band Aid Antiseptic Cleansing	BENZALKONIUM CHLORIDE	Kenvue Brands LLC	d3190050-d646-5957-e053-2995a90ad521	2025-04-08	Warnings	Exact identifier application number: M003
mart Care Assorted Hand Sanitizer 0.94oz-Sweet Pea 01	ALCOHOL	Shenzhen Lantern Scicence Co.,Ltd.	322b90e8-be38-7237-e063-6394a90a488f	2025-04-07	Warnings	Exact identifier application number: M003
Meijer Hydrating Hand Sanitizer 1oz - Watermelon	ALCOHOL	Shenzhen Lantern Scicence Co.,Ltd.	322c0bdd-4dc5-52e7-e063-6294a90a1380	2025-04-07	Warnings	Exact identifier application number: M003
Meijer Hydrating Hand Sanitizer 1oz - Berry	ALCOHOL	Shenzhen Lantern Scicence Co.,Ltd.	322c56b0-7eb6-c33a-e063-6394a90a15fb	2025-04-07	Warnings	Exact identifier application number: M003
Meijer Hydrating Hand Sanitizer 1oz - Vanilla	ALCOHOL	Shenzhen Lantern Scicence Co.,Ltd.	322ce179-c528-0f62-e063-6394a90ac560	2025-04-07	Warnings	Exact identifier application number: M003
MEDI-FIRST First Aid Antiseptic	HYDROGEN PEROXIDE	Ultra Distributors Inc	b6f7b346-3d6b-5953-e053-2995a90a878f	2025-04-07	Warnings	Exact identifier application number: M003
MEDI-FIRST First Aid Antiseptic	ISOPROPYL ALCOHOL	Ultra Distributors Inc	b6c88941-9982-3a37-e053-2995a90a8a5a	2025-04-07	Warnings	Exact identifier application number: M003
Walgreens Max Strength Burn Gel	BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE	Walgreens Co.	25a1e89b-bafd-4770-e063-6294a90a14d2	2025-04-07	Warnings	Exact identifier application number: M003
Eye Wash	WATER	CMC Group Inc.	6158a1f5-a6bc-4a3e-9d1d-0a310d9dc561	2025-04-02	Warnings	Exact identifier application number: M003
Standard ANSI First Aid	WATER, BENZALKONIUM CHLORIDE, ISOPROPYL ALCOHOL, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, LIDOCAINE HYDROCHLORIDE	CMC Group, Inc.	e1ef74bf-8895-4200-a411-f726dcdaa945	2025-04-02	Warnings	Exact identifier application number: M003
Clear Defense	ETHYL ALCOHOL	Melaleuca, Inc.	a2178a68-780e-e69b-e053-2a95a90ab7d6	2025-04-02	Warnings	Exact identifier application number: M003
Large ANSI First Aid Kit	WATER, BENZALKONIUM CHLORIDE, ISOPROPYL ALCOHOL, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, LIDOCAINE HYDROCHLORIDE	CMC Group, Inc.	fa8578c2-a0bc-4e2e-a4f9-d48debfff378	2025-04-02	Warnings	Exact identifier application number: M003
ETHYL ALCOHOL	ALCOHOL	ASP Global LLC	67a4b949-ce8a-4841-a965-fcc94165135c	2025-04-02	Warnings	Exact identifier application number: M003
Sanitizing Hand Mist	ETHYL ALCOHOL	ALO New York LLC	31baefe1-2521-9ef3-e063-6294a90a450e	2025-04-01	Warnings	Exact identifier application number: M003
Deconimo	HAND SANITIZING WIPES	IMAGINE AMAZON LLC	311c670d-8f87-b746-e063-6294a90afd5e	2025-04-01	Warnings	Exact identifier application number: M003
Meijer Antibacterial Foaming Hand Wash	0.13% BENZALKONIUM CHLORIDE SOLUTION	Meijer, Inc.	1eb6b603-ef96-dfda-e063-6294a90ae468	2025-03-31	Warnings	Exact identifier application number: M003

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
ND2M416302	ISOPROPYL ALCOHOL	67-63-0	ISOPROPYL ALCOHOL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
797544	isopropyl alcohol 70 % Medicated Pad	PSN	6551187f-5cde-4149-931f-b057bd760750	11
797544	isopropyl alcohol 0.7 ML/ML Medicated Pad	SCD	6551187f-5cde-4149-931f-b057bd760750	11
797544	isopropyl alcohol 70 % Medicated Pad	SY	6551187f-5cde-4149-931f-b057bd760750	11
797544	isopropyl alcohol 70 % Topical Cloth	SY	6551187f-5cde-4149-931f-b057bd760750	11
797544	isopropyl alcohol 70 % Topical Swab	SY	6551187f-5cde-4149-931f-b057bd760750	11
797544	isopropyl alcohol 70 % Medicated Pad	PSN	4eca7228-4bfc-4b6c-839e-73b02faa4d54	1
797544	isopropyl alcohol 0.7 ML/ML Medicated Pad	SCD	4eca7228-4bfc-4b6c-839e-73b02faa4d54	1
797544	isopropyl alcohol 70 % Medicated Pad	SY	4eca7228-4bfc-4b6c-839e-73b02faa4d54	1
797544	isopropyl alcohol 70 % Topical Cloth	SY	4eca7228-4bfc-4b6c-839e-73b02faa4d54	1
797544	isopropyl alcohol 70 % Topical Swab	SY	4eca7228-4bfc-4b6c-839e-73b02faa4d54	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
30142-809-09	30142080909	100 in 1 BOX						Historical
30142-809-30	30142080930	100 PACKET in 1 BOX (30142-809-30) / 1 APPLICATOR in 1 PACKET / .5 mL in 1 APPLICATOR	100 packet	2010-03-31	0000-00-00	No	No	Current
30142-809-31	30142080931	140 PACKET in 1 BOX (30142-809-31) / 1 APPLICATOR in 1 PACKET / 1.5 mL in 1 APPLICATOR	140 packet	2010-03-31	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
30142-809 Kroger Alcohol Prep Pads	The Kroger Company \| Medline Industries, LP	2026-09-02	HUMAN OTC DRUG LABEL	12
Drug Facts	The Kroger Company	2010-03-31	HUMAN OTC DRUG LABEL	1