50% Rubbing

Product NDC: 11344-003
Requested package NDC: 11344-003-45
11-digit product format: 113440003
Labeler code: 11344
Product ID: 11344-003_86cb723d-4b3f-4bbe-bc46-d7270265f421
Type: HUMAN OTC DRUG
Nonproprietary name: Isopropyl Alcohol
Dosage form: LIQUID
Route: TOPICAL
Labeler: Sound Body
Application: part333A
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2014-10-08
Marketing end: 0000-00-00
Substance: ISOPROPYL ALCOHOL
Active strength: 500 mg/mL
NDC exclude flag: No
Listing certified through: 2022-12-31
Current FDA listing: Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	11344-003	11344-003-45	D	Discontinued by firm		2026-08-03

Observed NDC auxiliary status history#

Observed captured status history: Rows come only from successfully parsed FDA auxiliary ZIP captures. They show the state present in that artifact, not a continuous regulatory timeline. Absence before, after, or between captures is not proof of status, and a known non-data HTTP 403 capture is preserved in backfill provenance but cannot produce a status row.

Historic NDC status page 1 of 1 · 10 matching rows.

Browse every current auxiliary row. · Browse the complete NDC auxiliary source catalog.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Product NDC	Package NDC	Code	Status	Archive	Snapshot	Source SHA-256
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	11344-003	11344-003-45	I	Inactivated by FDA	excluded / ndc_excluded.zip	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	11344-003	11344-003-45	I	Inactivated by FDA	excluded / ndc_excluded.zip	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	11344-003	11344-003-45	I	Inactivated by FDA	excluded / ndc_excluded.zip	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	11344-003	11344-003-45	I	Inactivated by FDA	excluded / ndc_excluded.zip	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	11344-003	11344-003-45	I	Inactivated by FDA	excluded / ndc_excluded.zip	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	11344-003	11344-003-45	I	Inactivated by FDA	excluded / ndc_excluded.zip	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	11344-003	11344-003-45	I	Inactivated by FDA	excluded / ndc_excluded.zip	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded package	package	11344-003	11344-003-45	I	Inactivated by FDA	excluded / ndc_excluded.zip	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	11344-003	11344-003-45	I	Inactivated by FDA	excluded / ndc_excluded.zip	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	11344-003	11344-003-45	I	Inactivated by FDA	excluded / ndc_excluded.zip	`1332a3947898…`	`d4bfe170f9cd…`

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
11344-003-43	2025-11-01	C162847	48780-1	f386c649-c147-0266-e053-dadaa90a7c1a	Sound Body 864.003 864AC
11344-003-45	2025-11-01	C162847	48780-1	f386c649-c147-0266-e053-dadaa90a7c1a	Sound Body 864.003 864AC
11344-003-43	2023-01-30	C162847	48780-1	f386c649-c147-0266-e053-dadaa90a7c1a	Sound Body 864.003 864AC
11344-003-45	2023-01-30	C162847	48780-1	f386c649-c147-0266-e053-dadaa90a7c1a	Sound Body 864.003 864AC

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ISOPROPYL ALCOHOL	ACTIVE INGREDIENT	ND2M416302	50% RUBBING (ISOPROPYL ALCOHOL) LIQUID [SOUND BODY]	1
ISOPROPYL ALCOHOL	ACTIVE MOIETY	ND2M416302	50% RUBBING (ISOPROPYL ALCOHOL) LIQUID [SOUND BODY]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	50% RUBBING (ISOPROPYL ALCOHOL) LIQUID [SOUND BODY]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
11344-003	50% RUBBING (ISOPROPYL ALCOHOL) LIQUID [SOUND BODY]	11	Legacy NDC	20210520_cea74c5e-ef73-473d-bdd0-449394f798a1.zip

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

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
11344-003-45	11344000345	946 mL in 1 BOTTLE, PLASTIC (11344-003-45)	946 ml	2014-10-08	0000-00-00	No	No	Current