NDC 63779-514

HUSKY 514 Non-Alcohol Foaming Instant Hand Sanitizer

Husky 514

HUSKY 514 Non-Alcohol Foaming Instant Hand Sanitizer is a Topical Solution in the Human Otc Drug category. It is labeled and distributed by Canberra Corporation. The primary component is Benzalkonium Chloride.

• Product ID: 63779-514_18e58373-40c4-4b4c-b868-a18eadf96e52
• NDC: 63779-514
• Product Type: Human Otc Drug
• Proprietary Name: HUSKY 514 Non-Alcohol Foaming Instant Hand Sanitizer
• Generic Name: Husky 514
• Dosage Form: Solution
• Route of Administration: TOPICAL
• Marketing Start Date: 2009-11-16
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part333
• Labeler Name: Canberra Corporation
• Substance Name: BENZALKONIUM CHLORIDE
• Active Ingredient Strength: 1 g/1000mL
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 63779-514-99

250 mL in 1 BOTTLE (63779-514-99)

• Marketing Start Date: 2009-11-16
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 63779-514-99 [63779051499]

HUSKY 514 Non-Alcohol Foaming Instant Hand Sanitizer SOLUTION

• Marketing Category: OTC monograph not final
• Application Number: part333
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2009-11-16
• Inactivation Date: 2019-10-21

NDC 63779-514-82 [63779051482]

HUSKY 514 Non-Alcohol Foaming Instant Hand Sanitizer SOLUTION

• Marketing Category: OTC monograph not final
• Application Number: part333
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2009-11-16
• Inactivation Date: 2019-10-21

NDC 63779-514-10 [63779051410]

HUSKY 514 Non-Alcohol Foaming Instant Hand Sanitizer SOLUTION

• Marketing Category: OTC monograph not final
• Application Number: part333
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2009-11-16
• Inactivation Date: 2019-10-21

NDC 63779-514-42 [63779051442]

HUSKY 514 Non-Alcohol Foaming Instant Hand Sanitizer SOLUTION

• Marketing Category: OTC monograph not final
• Application Number: part333
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2009-11-16
• Inactivation Date: 2019-10-21

Drug Details

Active Ingredients

Ingredient	Strength
BENZALKONIUM CHLORIDE	1 g/1000mL

OpenFDA Data

• SPL SET ID: c70284c1-6172-4db0-9c9e-b1e4158ffa41
• Manufacturer:
  • Canberra Corporation
• UNII:
  • F5UM2KM3W7
• RxNorm Concept Unique ID - RxCUI:
  • 1038799

NDC Crossover Matching brand name "HUSKY 514 Non-Alcohol Foaming Instant Hand Sanitizer" or generic name "Husky 514"

NDC	Brand Name	Generic Name
63779-514	HUSKY 514 Non-Alcohol Foaming Instant Hand Sanitizer	Husky 514
50112-514	Envirokleen Non-Alcohol Instant Hand Sanitizer	Husky 514
50036-514	Fikes Northwest Non-Alcohol Foaming Instant Hand Sanitizer	Husky 514
43196-514	OPI Personal Care Supplies Instant Foaming Hand Sanitizer Non Alcohol	Husky 514
62065-514	Sport Mate Non-Alcohol Foaming Instant Hand Sanitizer	HUSKY 514