Sanitizer Wipe in Sachet

Product NDC: 69491-035
11-digit product format: 694910035
Labeler code: 69491
Product ID: 69491-035_f114c712-b498-245f-e053-2995a90a79cc
Type: HUMAN OTC DRUG
Nonproprietary name: ALCOHOL
Dosage form: CLOTH
Route: TOPICAL
Labeler: Buzz Export Services Pty Ltd (Buzz Products)
Application: part333E
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2022-02-15
Marketing end: 0000-00-00
Substance: ALCOHOL
Active strength: 75 mL/100mL
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	69491-035		D	Discontinued by firm		2026-10-05
excluded package	package	69491-035	69491-035-01	D	Discontinued by firm		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 · 22 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	69491-035-01	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	69491-035-01	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	69491-035-01	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	69491-035-01	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	69491-035-01	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	69491-035-01	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	69491-035-01	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	69491-035-01	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	69491-035-01	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	69491-035-01	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	69491-035-01	`367a005e9d99…`	`383a685ebd0f…`

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
69491-035-01	2024-07-30	C162847	48780-1	1e7a6dab-19f7-a2ce-e063-dadaa90aadf7	Sanitizer Wipe in Sachet

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69491-035	SANITIZER WIPE IN SACHET (ALCOHOL) CLOTH [BUZZ EXPORT SERVICES PTY LTD (BUZZ PRODUCTS)]	3	Legacy NDC	20231221_d31db1e4-77e5-838c-e053-2995a90a6872.zip
69491-035	UNITED AIRLINES POLARIS KIT (SODIUM MONOFLUOROPHOSPHATE, ALCOHOL) KIT [BUZZ EXPORT SERVICES PTY LTD (BUZZ PRODUCTS)]	3	Legacy NDC	20241025_d31dd3b7-e669-6506-e053-2995a90a03d0.zip
69491-035	UNITED AIRLINES TRANSCON KIT (SODIUM MONOFLUOROPHOSPHATE, ALCOHOL) KIT [BUZZ EXPORT SERVICES PTY LTD (BUZZ PRODUCTS)]	3	Legacy NDC	20241025_d31def51-2c20-3006-e053-2995a90accba.zip
69491-035	UNITED AIRLINES UPP KIT (SODIUM MONOFLUOROPHOSPHATE, ALCOHOL) KIT [BUZZ EXPORT SERVICES PTY LTD (BUZZ PRODUCTS)]	3	Legacy NDC	20241025_d31e0262-1c49-29a1-e053-2995a90ab67c.zip

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
69491-035-01	69491003501	1 PATCH in 1 PACKAGE (69491-035-01) > 5 mL in 1 PATCH	1 patch	2022-02-15	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
United Airlines Polaris Kit	Buzz Products Inc	2026-03-11	HUMAN OTC DRUG LABEL	4
United Airlines Transcon Kit	Buzz Products Inc.	2026-03-11	HUMAN OTC DRUG LABEL	4
Sanitizer Wipe in Sachet	Buzz Export Services Pty Ltd (Buzz Products)	2023-12-20	HUMAN OTC DRUG LABEL	3
United Airlines UPP Kit	Buzz Export Services Pty Ltd (Buzz Products)	2023-12-20	HUMAN OTC DRUG LABEL	3