NDC 50663-003

Hand Sanitizer-Gel

Dial Professional Gel Hand Sanitizer

Hand Sanitizer-Gel is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Zotos International Inc. The primary component is Alcohol.

Product ID50663-003_a44cec41-bb92-811f-e053-2a95a90a1885
NDC50663-003
Product TypeHuman Otc Drug
Proprietary NameHand Sanitizer-Gel
Generic NameDial Professional Gel Hand Sanitizer
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2020-05-01
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart356
Labeler NameZotos International Inc
Substance NameALCOHOL
Active Ingredient Strength60 mL/100mL
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 50663-003-01

118 mL in 1 BOTTLE (50663-003-01)
Marketing Start Date2020-05-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50663-003-05 [50663000305]

Hand Sanitizer-Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart356
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-05-01

NDC 50663-003-01 [50663000301]

Hand Sanitizer-Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart356
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-05-01

NDC 50663-003-03 [50663000303]

Hand Sanitizer-Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart356
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-05-01

NDC 50663-003-02 [50663000302]

Hand Sanitizer-Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart356
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-05-01

NDC 50663-003-04 [50663000304]

Hand Sanitizer-Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart356
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-05-01

Drug Details

Active Ingredients

IngredientStrength
ALCOHOL60.146532 mL/100mL

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.