NDC 76687-005

V W

Advance Hand Sanitizer

V W is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Val Usa Manufacturer Inc. The primary component is Alcohol.

Product ID76687-005_a496764a-9613-f40c-e053-2995a90aaa5e
NDC76687-005
Product TypeHuman Otc Drug
Proprietary NameV W
Generic NameAdvance Hand Sanitizer
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2020-05-15
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333A
Labeler NameVAL USA Manufacturer Inc
Substance NameALCOHOL
Active Ingredient Strength75 mL/100mL
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 76687-005-01

30 mL in 1 BOTTLE (76687-005-01)
Marketing Start Date2020-05-15
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 76687-005-03 [76687000503]

V W GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-05-15

NDC 76687-005-05 [76687000505]

V W GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-05-15

NDC 76687-005-13 [76687000513]

V W GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-05-15

NDC 76687-005-08 [76687000508]

V W GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-05-15

NDC 76687-005-16 [76687000516]

V W GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-05-15

NDC 76687-005-12 [76687000512]

V W GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-05-15

NDC 76687-005-04 [76687000504]

V W GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-05-15

NDC 76687-005-07 [76687000507]

V W GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-05-15

NDC 76687-005-19 [76687000519]

V W GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-05-15

NDC 76687-005-02 [76687000502]

V W GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-05-15

NDC 76687-005-01 [76687000501]

V W GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-05-15

NDC 76687-005-09 [76687000509]

V W GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-05-15

NDC 76687-005-14 [76687000514]

V W GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-05-15

NDC 76687-005-20 [76687000520]

V W GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-05-15

NDC 76687-005-11 [76687000511]

V W GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-05-15

NDC 76687-005-18 [76687000518]

V W GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-05-15

NDC 76687-005-17 [76687000517]

V W GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-05-15

NDC 76687-005-15 [76687000515]

V W GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-05-15

NDC 76687-005-06 [76687000506]

V W GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-05-15

NDC 76687-005-10 [76687000510]

V W GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-05-15

Drug Details

NDC Crossover Matching brand name "V W" or generic name "Advance Hand Sanitizer"

NDCBrand NameGeneric Name
75239-006V WAdvance Hand Sanitizer
75239-007V WHand Sanitizer Wipe
76687-005V WAdvance Hand Sanitizer
76687-006V WAdvance Hand Sanitizer
76687-008V WAdvance Hand Sanitizer
75239-005Advance Hand SanitizerAdvance Hand Sanitizer

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