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		2026-10-15
excluded package	package	76309-301	76309-301-88	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 · 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 39 of 115 · 2,286 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Hand sanitizer	HAND SANITIZER SPRAY	Beimei Biotechnology (Guangzhou) Co., Ltd.	49455156-1072-14f5-e063-6294a90abdff	2026-01-26	Warnings	Exact identifier application number: M003
Anti-bacterial Hand Wipes	ANTI-BACTERIAL HAND WIPES	Jinhua Aidi Daily Chemical Co., Ltd.	494b09a4-4982-13bf-e063-6394a90a486f	2026-01-26	Warnings	Exact identifier application number: M003
Homworks Alcohol Wipes Multipurpose	ETHYL ALCOHOL	Acadian Crossing Consumer Products, LLC.	c9f0c3b3-5f39-dfa6-e053-2995a90a7644	2026-01-26	Warnings	Exact identifier application number: M003
BZK Pads	BENZALKONIUM CHLORIDE	Dynarex Corporation	87288939-cc34-4437-94ab-dcb997d6acd5	2026-01-23	Warnings	Exact identifier application number: M003
BZK Pads	BENZALKONIUM CHLORIDE	Dynarex Corporation	10454042-ff2e-44ce-b2e2-436cc004897f	2026-01-23	Warnings	Exact identifier application number: M003
Everlit Survival Sting Relief Pad	ISOPROPYL ALCOHOL	EVERLIT GLOBAL INC.	3a0414ea-f862-aa0f-e063-6294a90aecb7	2026-01-23	Warnings	Exact identifier application number: M003
Medline	POVIDONE-IODINE	Medline Industries, LP	48ebfdd6-d346-7e26-e063-6394a90af11a	2026-01-23	Warnings	Exact identifier application number: M003
EVERLIT SURVIVAL IODINE PREP PADS	POVIDONE-IODINE	EVERLIT GLOBAL INC.	3a03fc8d-2653-9183-e063-6294a90ad76e	2026-01-23	Warnings	Exact identifier application number: M003
EVERLIT SURVIVAL PREP PAD	ISOPROPYL ALCOHOL	EVERLIT GLOBAL INC.	3a03ed81-5b1d-172e-e063-6394a90ac59c	2026-01-23	Warnings	Exact identifier application number: M003
Everlit Survival Antiseptic Wipe	ANTISEPTIC WIPE	EVERLIT GLOBAL INC.	3a03f7e6-cc74-22a2-e063-6394a90a5f9f	2026-01-23	Warnings	Exact identifier application number: M003
Rite Aid Isopropyl Alcohol Wipes	ISOPROPYL ALCOHOL	Rite Aid	bca837b0-5044-4e97-e053-2a95a90a13af	2026-01-22	Warnings	Exact identifier application number: M003
Drs. Pharmacy Triple Antibiotic AND BURN RELIEF	BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE	OL PHARMA TECH, LLC Drs PHARMACY	4928d9dd-542b-fe8b-e063-6294a90a9252	2026-01-22	Warnings	Exact identifier application number: M003
DOP Ethyl Alcohol 70%	ETHYL ALCOHOL	Omega & Delta Co., Inc.	b96d85f8-739c-4b96-9dd5-8119ebf66c9f	2026-01-21	Warnings	Exact identifier application number: M003
AshleyBelle Moisturizing Hand Sanitizer Rose Lychee	ETHYL ALCOHOL	Zhejiang Guoyao Jingyue Aerosol Co., Ltd.	48dfcbe1-8e0c-1715-e063-6394a90a733f	2026-01-21	Warnings	Exact identifier application number: M003
Lights Povindone Iodine Swabstick	POVIDONE-IODINE	Lights Medical Manufacture Co., Ltd.	977b6077-bf47-4e02-bde4-c752e73d7628	2026-01-21	Warnings	Exact identifier application number: M003
Lights Povindone Iodine Scrub	POVIDONE-IODINE	Lights Medical Manufacture Co., Ltd.	000bf57b-1805-4746-bf1c-32856241213a	2026-01-21	Warnings	Exact identifier application number: M003
Lights Povidone Iodine Solution	POVIDONE-IODINE	Lights Medical Manufacture Co., Ltd.	6946eb98-6870-4b21-9dda-b01a8adab84b	2026-01-21	Warnings	Exact identifier application number: M003
Lights Povidone Iodine Prep Pad	POVIDONE-IODINE	Lights Medical Manufacture Co., Ltd.	e561332d-e419-43db-a68e-0c0d49b01c9a	2026-01-21	Warnings	Exact identifier application number: M003
Lights Povindone Iodine Swabstick	POVIDONE-IODINE	Lights Medical Manufacture Co., Ltd.	2610fde4-4572-4d15-a970-f6d3beb734fe	2026-01-21	Warnings	Exact identifier application number: M003
Lights Povidone Iodine Solution	POVIDONE-IODINE	Lights Medical Manufacture Co., Ltd.	7d4a92be-0601-4256-bc5b-bc1b07d97bb7	2026-01-21	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