Alcohol

Product NDC: 64024-849
11-digit product format: 640240849
Labeler code: 64024
Product ID: 64024-849_498c60b0-32a4-b619-e063-6294a90a7d59
Type: HUMAN OTC DRUG
Nonproprietary name: Alcohol
Dosage form: LIQUID
Route: TOPICAL
Labeler: Aldi, Inc
Application: 505G(a)(3)
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2020-12-20
Substance: ALCOHOL
Active strength: 62 mg/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	64024-849	64024-849-16	D	Discontinued by firm		2026-08-17
excluded package	package	64024-849	64024-849-45	D	Discontinued by firm		2026-08-17

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 · 14 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	64024-849-45	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	64024-849-16	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	64024-849-45	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	64024-849-16	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	64024-849-45	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	64024-849-16	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	64024-849-45	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	64024-849-16	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	64024-849-45	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	64024-849-16	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	64024-849-45	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	64024-849-16	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	64024-849-45	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	64024-849-16	`302b2466d912…`	`e7b80fea0513…`

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ALCOHOL	62 mg/100mL

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
aaa55815-ab6d-41c0-b04f-53de8001ebc7	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
64024-849-16	Alcohol	59 mL in 1 BOTTLE, PLASTIC	LIQUID	59	5
64024-849-34	Alcohol	236 mL in 1 BOTTLE, PLASTIC	LIQUID	236	5
64024-849-45	Alcohol	946 mL in 1 BOTTLE, PLASTIC	LIQUID	946	5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
64024-849	ALCOHOL LIQUID [ALDI INC.]	4	Current NDC, Legacy NDC, 3 package rows	20250129_aaa55815-ab6d-41c0-b04f-53de8001ebc7.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 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Alcohol	ALCOHOL	Aldi, Inc	aaa55815-ab6d-41c0-b04f-53de8001ebc7	2026-01-29	Warnings	Exact identifier ndc (product): 64024-849

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
64024-849-16	64024084916	59 mL in 1 BOTTLE, PLASTIC (64024-849-16)	59 ml	2020-12-20	0000-00-00	No	No	Current
64024-849-34	64024084934	236 mL in 1 BOTTLE, PLASTIC (64024-849-34)	236 ml	2020-12-20	0000-00-00	No	No	Current
64024-849-45	64024084945	946 mL in 1 BOTTLE, PLASTIC (64024-849-45)	946 ml	2020-12-20	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Lacura 849.001/849AE Moisturizing Hand Sanitizer	Aldi, Inc \| Nice-Pak Products, LLC	2026-01-29	HUMAN OTC DRUG LABEL	5