V W

Product NDC: 76687-008
Requested package NDC: 76687-008-20
11-digit product format: 766870008
Labeler code: 76687
Product ID: 76687-008_c950b86d-8ffb-d638-e053-2a95a90a4894
Type: HUMAN OTC DRUG
Nonproprietary name: Advance Hand Sanitizer
Dosage form: GEL
Route: TOPICAL
Labeler: VAL USA Manufacturer Inc
Application: part333A
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2020-05-10
Marketing end: 0000-00-00
Substance: ALCOHOL
Active strength: 75 mL/100mL
NDC exclude flag: No
Listing certified through: 2022-12-31
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	76687-008	76687-008-20	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 · 15 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	`1332a3947898…`	`d4bfe170f9cd…`

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Related label table
NDC	Related label
76687-008-01	VAL-GEL
76687-008-02	VAL-GEL
76687-008-03	VAL-GEL
76687-008-04	VAL-GEL
76687-008-05	VAL-GEL
76687-008-06	VAL-GEL
76687-008-07	VAL-GEL
76687-008-08	VAL-GEL
76687-008-09	VAL-GEL
76687-008-10	VAL-GEL
76687-008-11	VAL-GEL
76687-008-12	VAL-GEL
76687-008-13	VAL-GEL
76687-008-14	VAL-GEL
76687-008-15	VAL-GEL
76687-008-16	VAL-GEL
76687-008-17	VAL-GEL
76687-008-18	VAL-GEL
76687-008-19	VAL-GEL
76687-008-20	VAL-GEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
76687-008-01	V W	30 mL in 1 BOTTLE	GEL	30	4
76687-008-02	V W	50 mL in 1 BOTTLE	GEL	50	4
76687-008-03	V W	80 mL in 1 BOTTLE	GEL	80	4
76687-008-04	V W	100 mL in 1 BOTTLE	GEL	100	4
76687-008-05	V W	120 mL in 1 BOTTLE	GEL	120	4
76687-008-06	V W	150 mL in 1 BOTTLE	GEL	150	4
76687-008-07	V W	180 mL in 1 BOTTLE	GEL	180	4
76687-008-08	V W	200 mL in 1 BOTTLE	GEL	200	4
76687-008-09	V W	240 mL in 1 BOTTLE	GEL	240	4
76687-008-10	V W	250 mL in 1 BOTTLE	GEL	250	4
76687-008-11	V W	300 mL in 1 BOTTLE	GEL	300	4
76687-008-12	V W	350 mL in 1 BOTTLE	GEL	350	4
76687-008-13	V W	500 mL in 1 BOTTLE	GEL	500	4
76687-008-14	V W	650 mL in 1 BOTTLE	GEL	650	4
76687-008-15	V W	1000 mL in 1 BOTTLE	GEL	1000	4
76687-008-16	V W	3800 mL in 1 BOTTLE	GEL	3800	4
76687-008-17	V W	5000 mL in 1 BOTTLE	GEL	5000	4
76687-008-18	V W	20000 mL in 1 BOTTLE	GEL	20000	4
76687-008-19	V W	50000 mL in 1 BOTTLE	GEL	50000	4
76687-008-20	V W	1000000 mL in 1 BOTTLE	GEL	1000000	4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
76687-008	V W (ADVANCE HAND SANITIZER) GEL [VAL USA MANUFACTURER INC]	4	Legacy NDC, 20 package rows	20210813_a4b906f5-70fe-030d-e053-2a95a90a2b34.zip

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
1305100	ethanol 75 % Topical Gel	PSN	a4b906f5-70fe-030d-e053-2a95a90a2b34	4
1305100	ethanol 0.75 ML/ML Topical Gel	SCD	a4b906f5-70fe-030d-e053-2a95a90a2b34	4
1305100	ethanol 75 % Topical Gel	SY	a4b906f5-70fe-030d-e053-2a95a90a2b34	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
76687-008-20	76687000820	1000000 mL in 1 BOTTLE (76687-008-20)	1000000 ml	2021-08-12	0000-00-00	No	No	Current

V W