70% Isopropyl Alcohol

Product NDC: 72288-810
11-digit product format: 722880810
Labeler code: 72288
Product ID: 72288-810_4cc0620d-aa92-0dac-e063-6294a90ad6c4
Type: HUMAN OTC DRUG
Nonproprietary name: Isopropyl alcohol
Dosage form: LIQUID
Route: TOPICAL
Labeler: Amazon.com Services LLC
Application: M003
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2018-05-01
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 package	package	72288-810	72288-810-43	D	Discontinued by firm		2026-10-20
excluded package	package	72288-810	72288-810-72	D	Discontinued by firm		2026-10-20

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 · 22 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Package NDC, Snapshot table
Captured / source date	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	72288-810-72	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	72288-810-43	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	72288-810-72	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	72288-810-43	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	72288-810-43	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	72288-810-72	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	72288-810-43	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	72288-810-72	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	72288-810-43	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	72288-810-72	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	72288-810-43	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	72288-810-72	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	72288-810-43	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	72288-810-72	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	72288-810-43	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	72288-810-72	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	72288-810-43	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	72288-810-72	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	72288-810-43	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	72288-810-72	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	72288-810-43	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	72288-810-45	`367a005e9d99…`	`383a685ebd0f…`

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: 70% Isopropyl 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
808520	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
106f51fa-e687-470f-8ed8-35cb0565aeff	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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
72288-810-43	70% Isopropyl Alcohol	473 mL in 1 BOTTLE, PLASTIC	LIQUID	473	12
72288-810-45	70% Isopropyl Alcohol	946 mL in 1 BOTTLE, PLASTIC	LIQUID	946	12
72288-810-72	70% Isopropyl Alcohol	296 mL in 1 BOTTLE, SPRAY	LIQUID	296	12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72288-810	70% ISOPROPYL ALCOHOL (ISOPROPYL ALCOHOL) LIQUID [AMAZON.COM SERVICES LLC]	9	Current NDC, Legacy NDC, 3 package rows	20250521_106f51fa-e687-470f-8ed8-35cb0565aeff.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 104 of 115 · 2,286 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Swabs	ISOPROPYL ALCOHOL	McKesson	4650c945-8e38-5ad9-e054-00144ff8d46c	2024-06-07	Warnings	Exact identifier application number: M003
HAND SANITIZER COCONUT BREEZE	ALCOHOL	SCENT THEORY PRODUCTS LLC	1a5152b3-d674-f69a-e063-6394a90a6cac	2024-06-07	Warnings	Exact identifier application number: M003
HAND SANITIZER REBEL CHERRY	ALCOHOL	SCENT THEORY PRODUCTS LLC	1a503858-4d2f-8e32-e063-6294a90ade97	2024-06-07	Warnings	Exact identifier application number: M003
Antiseptic Wipe	BENZALKONIUM CHLORIDE	Jianerkang Medical Co., Ltd	1a3c5fc9-70cc-e857-e063-6294a90a3424	2024-06-06	Warnings	Exact identifier application number: M003
Hydrogen Peroxide	HYDROGEN PEROXIDE	Wildman Business Group	1f95b277-e40c-4a17-e063-6294a90a1127	2024-06-01	Warnings	Exact identifier application number: M003
Hand Sanitizer	ALCOHOL	JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.	dbfdecf0-a961-4cc5-bf87-ae30bbc302dd	2024-05-31	Warnings	Exact identifier application number: M003
hand sanitizer 01	ALCOHOL	Cosmuses Cosmetics (Ningbo) Co., Ltd.	19a6c3c6-4b27-9011-e063-6394a90ae512	2024-05-30	Warnings	Exact identifier application number: M003
antibacterial hand sanitizer gel 01	ALCOHOL	Cosmuses Cosmetics (Ningbo) Co., Ltd.	19a7b2fc-239c-b53c-e063-6394a90a0906	2024-05-30	Warnings	Exact identifier application number: M003
MyMedic Hydrocortisone	HYDROCORTISONE	Nantong Health & Beyond Hygienic Products Inc.	197fc623-2fb9-184c-e063-6394a90a4104	2024-05-28	Warnings	Exact identifier application number: M003
Nourishing Hand Sanitizer Limon	ALCOHOL	Noshinku	d70fba7a-513f-0341-e053-2a95a90add86	2024-05-15	Warnings	Exact identifier application number: M003
Nourishing Hand Sanitizer Vetiver	ALCOHOL	Noshinku	d70fb84c-fdbc-6ba8-e053-2995a90ab529	2024-05-15	Warnings	Exact identifier application number: M003
Safly BZK Antiseptic Towelette	BENZALKONIUM CHLORIDE	JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.	5cd9043e-daf2-43eb-9568-54775fc4f84a	2024-05-15	Warnings	Exact identifier application number: M003
Noshinku Bergamot Hand Sanitizer	ALCOHOL	Noshinku	53fea81e-4482-6fae-e054-00144ff8d46c	2024-05-14	Warnings	Exact identifier application number: M003
Noshinku Eucalyptus Hand Sanitizer	ALCOHOL	Noshinku	9dcb8b51-d1bb-4305-a5ff-8cc8bdcdc4c0	2024-05-14	Warnings	Exact identifier application number: M003
Noshinku Lavender Hand Sanitizer	ALCOHOL	Noshinku	a57e44b2-f5fa-4c3c-a59c-aa73bfbb66cf	2024-05-14	Warnings	Exact identifier application number: M003
LEADER 2% Mild Iodine Tincture	IODINE AND SODIUM IODIDE AND ALCOHOL LIQUID	Cardinal Health, 110 dba Leader	7f810b92-60f6-2f72-e053-2991aa0ab973	2024-05-13	Warnings	Exact identifier application number: M003
Leader Decolorized Iodine	ALCOHOL LIQUID	Cardinal Health, 110 dba Leader	822f6f28-956f-dd82-e053-2991aa0ae752	2024-05-13	Warnings	Exact identifier application number: M003
Inverness Ear Care	BENZALKONIUM CHLORIDE	The Richline Group, Inc.	180a2995-334c-2e93-e063-6294a90aecf7	2024-05-09	Warnings	Exact identifier application number: M003
Helzberg Diamonds Ear Care	BENZALKONIUM CHLORIDE	The Richline Group, Inc.	180a3776-0edd-26f3-e063-6294a90a740d	2024-05-09	Warnings	Exact identifier application number: M003
Ulta Beauty Ear Care	BENZALKONIUM CHLORIDE	The Richline Group, Inc.	180a37f4-8718-3e40-e063-6294a90acaad	2024-05-09	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
808520	isopropyl alcohol 70 % Topical Solution	PSN	106f51fa-e687-470f-8ed8-35cb0565aeff	12
808520	isopropyl alcohol 0.7 ML/ML Topical Solution	SCD	106f51fa-e687-470f-8ed8-35cb0565aeff	12
808520	isopropyl alcohol 70 % Topical Solution	SY	106f51fa-e687-470f-8ed8-35cb0565aeff	12

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
72288-810-43	72288081043	473 mL in 1 BOTTLE, PLASTIC (72288-810-43)	473 ml	2018-05-01	0000-00-00	No	No	Current
72288-810-45	72288081045	946 mL in 1 BOTTLE, PLASTIC (72288-810-45)	946 ml	2018-05-01		No	No	Current
72288-810-72	72288081072	296 mL in 1 BOTTLE, SPRAY (72288-810-72)	296 ml	2018-05-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Basics_Solimo 810.003/810AA Isopropyl Alcohol 70%	Amazon.com Services LLC \| Nice-Pak Products, LLC	2026-03-11	HUMAN OTC DRUG LABEL	12