SnugZ Hand Sanitizer Gel

Product NDC: 76309-301
11-digit product format: 763090301
Labeler code: 76309
Product ID: 76309-301_4720ba94-cc7c-fec5-e063-6394a90a59cb
Type: HUMAN OTC DRUG
Nonproprietary name: Hand Sanitizer Gel
Dosage form: GEL
Route: TOPICAL
Labeler: SnugZ/USA, LLC
Application: M003
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2018-01-01
Substance: ALCOHOL
Active strength: 70 mL/100mL
NDC exclude flag: No
Listing certified through: 2026-12-31
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	76309-301	76309-301-62	D	Discontinued by firm		2026-10-05
excluded package	package	76309-301	76309-301-88	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 · 24 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	76309-301-62	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	76309-301-88	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	76309-301-62	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	76309-301-88	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	76309-301-62	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	76309-301-88	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	76309-301-62	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	76309-301-88	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	76309-301-62	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	76309-301-88	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	76309-301-62	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	76309-301-88	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	76309-301-62	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	76309-301-88	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	76309-301-62	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	76309-301-88	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	76309-301-62	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	76309-301-88	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	76309-301-62	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	76309-301-88	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	76309-301-62	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	76309-301-88	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	76309-301-62	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	76309-301-88	`557ba5c1ecfa…`	`9c80585c8c6e…`

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: SnugZ Hand Sanitizer Gel
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ALCOHOL	70 mL/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 RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
581662	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
69bc7a80-0898-4c08-e053-2a91aa0a87a9	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
76309-301-01	SnugZ Hand Sanitizer Gel	28 mL in 1 BOTTLE	GEL	28	11
76309-301-02	SnugZ Hand Sanitizer Gel	56 mL in 1 BOTTLE	GEL	56	11
76309-301-04	SnugZ Hand Sanitizer Gel	112 mL in 1 BOTTLE	GEL	112	11
76309-301-05	SnugZ Hand Sanitizer Gel	14 mL in 1 BOTTLE	GEL	14	11
76309-301-08	SnugZ Hand Sanitizer Gel	224 mL in 1 BOTTLE, PUMP	GEL	224	11
76309-301-19	SnugZ Hand Sanitizer Gel	56 mL in 1 BOTTLE	GEL	56	11
76309-301-51	SnugZ Hand Sanitizer Gel	30 mL in 1 TUBE	GEL	30	11
76309-301-61	SnugZ Hand Sanitizer Gel	39.75 mL in 1 POUCH	GEL	39.75	11
76309-301-62	SnugZ Hand Sanitizer Gel	85.17 mL in 1 POUCH	GEL	85.17	11
76309-301-81	SnugZ Hand Sanitizer Gel	28 mL in 1 BOTTLE	GEL	28	11
76309-301-88	SnugZ Hand Sanitizer Gel	112 mL in 1 POUCH	GEL	112	11
76309-301-91	SnugZ Hand Sanitizer Gel	28 mL in 1 BOTTLE	GEL	28	11
76309-301-99	SnugZ Hand Sanitizer Gel	3785.41 mL in 1 JUG	GEL	3785.41	11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
76309-301	SNUGZ HAND SANITIZER GEL (HAND SANITIZER GEL) GEL [SNUGZ/USA, LLC]	10	Current NDC, Legacy NDC, 13 package rows	20241228_69bc7a80-0898-4c08-e053-2a91aa0a87a9.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 2 of 117 · 2,333 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Meijer	ISOPROPYL ALCOHOL	Meijer Distribution Inc	ca008d84-cf51-3703-e053-2a95a90a9bf1	2026-09-04	Warnings	Exact identifier application number: M003
Walmart	ISOPROPYL ALCOHOL	Walmart, Inc.	2eff98ba-5736-b07e-e063-6394a90aeea9	2026-09-04	Warnings	Exact identifier application number: M003
Walgreen Alcohol	ISOPROPYL ALCOHOL	Walgreens Company	deeae1ea-3d81-4260-95be-c4f328e3fdef	2026-09-04	Warnings	Exact identifier application number: M003
Dollar General	ISOPROPYL ALCOHOL	Dollar General Corporation	00b2ef34-42d9-523c-e063-6294a90a753d	2026-09-03	Warnings	Exact identifier application number: M003
Signature Select Alcohol Prep Pads	ISOPROPYL ALCOHOL	Better Living Brands LLC	31ce72e3-03a3-1608-e063-6394a90ad850	2026-09-03	Warnings	Exact identifier application number: M003
SurviveX Sting Relief	STING RELIEF WIPE	Changzhou Maokang Medical Products Co., Ltd.	5a83b1f1-c8dc-cf07-e063-6394a90a20ca	2026-09-03	Warnings	Exact identifier application number: M003
Benzethonium chloride Plus Dyclonine hydrochloride	LIQUID BANDAGE	Kroger Co.	fe604470-917f-4cbd-a1e6-ac1dc7c57ff6	2026-09-02	Warnings	Exact identifier application number: M003
Alcohol	ISOPROPYL ALCOHOL	Rite Aid Corporation	5104f9ab-0b28-449f-a55a-5438713a24df	2026-09-02	Warnings	Exact identifier application number: M003
Hydrogen Peroxide	HYDROGEN PEROXIDE	UpLift Brands, LLC	5a81b635-d188-0b29-e063-6294a90a1e4b	2026-09-02	Warnings, Adverse reactions	Exact identifier application number: M003
Hydrogen Peroxide	HYDROGEN PEROXIDE	CVS Pharmacy, Inc.	7f518646-c8fe-499a-b5e4-8e5a5a90e01d	2026-09-02	Warnings, Adverse reactions	Exact identifier application number: M003
Alcohol	ISOPROPYL ALCOHOL	The Kroger Company	6551187f-5cde-4149-931f-b057bd760750	2026-09-02	Warnings	Exact identifier application number: M003
Unscented NasalGuard Antiseptic Topical	BENZALKONIUM CHLORIDE	TRUTEK CORP.	eb036e11-a28c-fdc0-e053-2a95a90a9cdb	2026-09-02	Warnings	Exact identifier application number: M003
Harris Teeter	ISOPROPYL ALCOHOL	Harris Teeter, LLC	d2bb20bd-ec83-8d80-e053-2a95a90a2bba	2026-09-02	Warnings	Exact identifier application number: M003
School Health	ISOPROPYL ALCOHOL	School Health Corporation	db5d0b22-f2d7-23e5-e053-2a95a90aeb51	2026-09-02	Warnings	Exact identifier application number: M003
Alcohol Prep Pads	ISOPROPYL ALCOHOL	Topco Associates	2642298f-607e-fdca-e063-6394a90a69d9	2026-09-02	Warnings	Exact identifier application number: M003
HUSTLE BUTTER NUMBING	LIDOCAINE HCL, BENZALKONIUM CHLORIDE	H.B.D. DIST. INC.	5b4d0390-dac6-4a71-9fdc-5c31543e7c5a	2026-09-02	Warnings	Exact identifier application number: M003
NasalGuard Antiseptic Topical Cool Menthol	BENZALKONIUM CHLORIDE	TRUTEK CORP.	e9fd3ef8-78ff-6c9f-e053-2a95a90a21a8	2026-09-01	Warnings	Exact identifier application number: M003
Maximum Strength Betadine Clear	BENZALKONIUM CL AND PRAMOXINE HCL	Atlantis Consumer Healthcare, Inc.	31b94a76-1536-47c0-ab03-e487c2625c58	2026-08-31	Warnings	Exact identifier application number: M003
Biopure Antibacterial Hand Wipe	ANTIBACTERIAL HAND WIPE	Fujian Yifa Healthcare Products Co., Ltd.	5a28101f-ea8e-6071-e063-6294a90aad91	2026-08-31	Warnings	Exact identifier application number: M003
Biopure Antibacterial Hand Wipe	ANTIBACTERIAL HAND WIPE	Fujian Yifa Healthcare Products Co., Ltd.	5a3e62ce-52dc-121b-e063-6294a90a898f	2026-08-31	Warnings	Exact identifier application number: M003

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
3K9958V90M	ALCOHOL	64-17-5	ALCOHOL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
581662	ethanol 70 % Topical Gel	PSN	69bc7a80-0898-4c08-e053-2a91aa0a87a9	11
581662	ethanol 0.7 ML/ML Topical Gel	SCD	69bc7a80-0898-4c08-e053-2a91aa0a87a9	11
581662	ethanol 70 % Topical Gel	SY	69bc7a80-0898-4c08-e053-2a91aa0a87a9	11
581662	ethyl alcohol 70 % Topical Gel	SY	69bc7a80-0898-4c08-e053-2a91aa0a87a9	11

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
76309-301-01	76309030101	28 mL in 1 BOTTLE (76309-301-01)	28 ml	2018-01-01	0000-00-00	No	No	Current
76309-301-02	76309030102	56 mL in 1 BOTTLE (76309-301-02)	56 ml	2018-01-01	0000-00-00	No	No	Current
76309-301-04	76309030104	112 mL in 1 BOTTLE (76309-301-04)	112 ml	2018-01-01	0000-00-00	No	No	Current
76309-301-05	76309030105	14 mL in 1 BOTTLE (76309-301-05)	14 ml	2018-01-01	0000-00-00	No	No	Current
76309-301-08	76309030108	224 mL in 1 BOTTLE, PUMP (76309-301-08)	224 ml	2018-01-01	0000-00-00	No	No	Current
76309-301-19	76309030119	56 mL in 1 BOTTLE (76309-301-19)	56 ml	2018-01-01	0000-00-00	No	No	Current
76309-301-51	76309030151	30 mL in 1 TUBE (76309-301-51)	30 ml	2018-01-01	0000-00-00	No	No	Current
76309-301-61	76309030161	39.75 mL in 1 POUCH (76309-301-61)	39.75 ml	2018-01-01	0000-00-00	No	No	Current
76309-301-62	76309030162	85.17 mL in 1 POUCH	85.17 ml					Historical
76309-301-81	76309030181	28 mL in 1 BOTTLE (76309-301-81)	28 ml	2018-01-01	0000-00-00	No	No	Current
76309-301-88	76309030188	112 mL in 1 POUCH	112 ml					Historical
76309-301-91	76309030191	28 mL in 1 BOTTLE (76309-301-91)	28 ml	2018-01-01	0000-00-00	No	No	Current
76309-301-99	76309030199	3785.41 mL in 1 JUG (76309-301-99)	3785.41 ml	2020-04-20	0000-00-00	No	No	Current