NDC 73842-002

Koi Hand Sanitizer

Ethyl Alcohol, 62%

Koi Hand Sanitizer is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Koi Cbd Llc. The primary component is Alcohol.

• Product ID: 73842-002_a33a7691-ceb7-a579-e053-2995a90a64d5
• NDC: 73842-002
• Product Type: Human Otc Drug
• Proprietary Name: Koi Hand Sanitizer
• Generic Name: Ethyl Alcohol, 62%
• Dosage Form: Gel
• Route of Administration: TOPICAL
• Marketing Start Date: 2020-04-13
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part333A
• Labeler Name: Koi CBD LLC
• Substance Name: ALCOHOL
• Active Ingredient Strength: 62 g/100mL
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 73842-002-01

59 mL in 1 BOTTLE, PUMP (73842-002-01)

• Marketing Start Date: 2020-04-13
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 73842-002-01 [73842000201]

Koi Hand Sanitizer GEL

• Marketing Category: OTC monograph not final
• Application Number: part333A
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2020-04-13

Drug Details

Active Ingredients

Ingredient	Strength
ALCOHOL	62 g/100mL

OpenFDA Data

• SPL SET ID: a33a7691-ceb6-a579-e053-2995a90a64d5
• Manufacturer:
  • Koi CBD LLC
• UNII:
  • 3K9958V90M
• RxNorm Concept Unique ID - RxCUI:
  • 581660
• UPC Code:
  • 0857321007207

NDC Crossover Matching brand name "Koi Hand Sanitizer" or generic name "Ethyl Alcohol, 62%"

NDC	Brand Name	Generic Name
73842-002	Koi Hand Sanitizer	Ethyl Alcohol, 62%
73842-003	Koi Hand Sanitizer	Ethyl Alcohol, 70%