Hand Wash

Product NDC: 21130-575
Requested package NDC: 21130-575-45
11-digit product format: 211300575
Labeler code: 21130
Product ID: 21130-575_d0f996a5-0119-40d4-b6da-a89a34b24a7b
Type: HUMAN OTC DRUG
Nonproprietary name: Benzalkonium chloride
Dosage form: LIQUID
Route: TOPICAL
Labeler: Better Living Brands LLC
Application: part333A
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2015-12-28
Marketing end: 0000-00-00
Substance: BENZALKONIUM CHLORIDE
Active strength: 1 mg/mL
NDC exclude flag: No
Listing certified through: 2023-12-31
Current FDA listing: Historical FDA.report record

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 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	21130-575	21130-575-45	D	Discontinued by firm		2026-10-15

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 · 2 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Archive	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	21130-575	21130-575-45	D	Discontinued by firm		excluded / ndc_excluded.zip	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	21130-575	21130-575-45	D	Discontinued by firm		excluded / ndc_excluded.zip	`f5e01cc5f278…`	`a2eaf40c39c3…`

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
21130-575-45	2022-08-25	C162847	48780-1	e4f33bdf-a05f-d8a0-e053-dadaa90a6e4e	Signature Care 575.002/575AD Pear Foaming Antibacterial Hand Wash
21130-575-45	2022-07-29	C162847	48780-1	e4f33bdf-a05f-d8a0-e053-dadaa90a6e4e	Signature Care 575.002/575AD Pear Foaming Antibacterial Hand Wash

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
21130-575	HAND WASH (BENZALKONIUM CHLORIDE) LIQUID [BETTER LIVING BRANDS LLC]	10	Legacy NDC	20240927_d52445e0-d47d-42ca-952b-2982e6e623df.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
F5UM2KM3W7	BENZALKONIUM CHLORIDE	8001-54-5	BENZALKONIUM CHLORIDE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
21130-575-45	21130057545	946 mL in 1 BOTTLE, PLASTIC (21130-575-45)	946 ml	2015-12-28	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Signature Care 575.002/575AD Pear Foaming Antibacterial Hand Wash	Better Living Brands LLC \| Consumer Product Partners, LLC	2024-09-25	HUMAN OTC DRUG LABEL	10