SANITIZING WIPES

Product NDC: 75670-003
11-digit product format: 756700003
Labeler code: 75670
Product ID: 75670-003_d8c0d4f2-21e0-1609-e053-2995a90aed15
Type: HUMAN OTC DRUG
Nonproprietary name: BENZALKONIUM CHLORIDE,Didecyldimonium Chloride
Dosage form: CLOTH
Route: TOPICAL
Labeler: SHANGHAI SANJUN GENERAL MERCHANDISE CO., LTD.
Application: part333A
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2020-06-09
Marketing end: 0000-00-00
Substance: BENZALKONIUM CHLORIDE; DIDECYLDIMONIUM CHLORIDE
Active strength: 0 g/100g; g/100g
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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	75670-003		I	Inactivated by FDA		2026-10-05
excluded package	package	75670-003	75670-003-02	I	Inactivated by FDA		2026-10-05

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 · 18 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	75670-003-02	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	75670-003-02	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	75670-003-02	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	75670-003-02	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	75670-003-02	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	75670-003-02	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	75670-003-02	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	75670-003-02	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	75670-003-02	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

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
75670-003-02	2025-01-30	C162847	48780-1	d6a99b39-db38-a426-e053-dadaa90af4c2	75670-003 sanitizing wipes 0.1%Benzalkonium Chloride 0.15% Didecyldimonium Chloride
75670-003-02	2022-02-24	C162847	48780-1	d6a99b39-db38-a426-e053-dadaa90af4c2	75670-003 sanitizing wipes 0.1%Benzalkonium Chloride 0.15% Didecyldimonium Chloride
75670-003-02	2022-01-28	C162847	48780-1	d6a99b39-db38-a426-e053-dadaa90af4c2	75670-003 sanitizing wipes 0.1%Benzalkonium Chloride 0.15% Didecyldimonium Chloride

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
75670-003-02	SANITIZING WIPES	50 in 1 BAG	CLOTH	50		2
75670-003-02	SANITIZING WIPES	24 in 1 CARTON	CLOTH	24		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
75670-003	SANITIZING WIPES (BENZALKONIUM CHLORIDE,DIDECYLDIMONIUM CHLORIDE) CLOTH [SHANGHAI SANJUN GENERAL MERCHANDISE CO., LTD.]	2	Legacy NDC, 2 package rows	20220225_a7a7ea81-d9f5-6d06-e053-2a95a90a1512.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
F5UM2KM3W7	BENZALKONIUM CHLORIDE	8001-54-5	BENZALKONIUM CHLORIDE
JXN40O9Y9B	DIDECYLDIMONIUM CHLORIDE	7173-51-5	DIDECYLDIMONIUM CHLORIDE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
75670-003-02	75670000302	24 BAG in 1 CARTON (75670-003-02) > 50 POUCH in 1 BAG > .0078 g in 1 POUCH	24 bag	2020-06-09	0000-00-00	No	No	Current