68609-575 NDC - SANI-FOAM INSTANT HAND SANITIZER ()

Drug Information

Product NDC: 68609-575

Proprietary Name: Sani-Foam Instant Hand Sanitizer

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: General Products & Supply, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:1/31/2004

Package Information

No. Package Code Package Description Billing Unit
168609-575-101000 mL in 1 CARTRIDGE (68609-575-10)
268609-575-121000 mL in 1 BAG (68609-575-12)
368609-575-13800 mL in 1 BAG (68609-575-13)
468609-575-143785 mL in 1 BOTTLE, PLASTIC (68609-575-14)
568609-575-15946 mL in 1 BOTTLE, PLASTIC (68609-575-15)
668609-575-16236 mL in 1 BOTTLE, PLASTIC (68609-575-16)
768609-575-17532 mL in 1 BOTTLE, PLASTIC (68609-575-17)
868609-575-1850 mL in 1 BOTTLE, PLASTIC (68609-575-18)
968609-575-24115 mL in 1 BOTTLE, PLASTIC (68609-575-24)
1068609-575-55208200 mL in 1 DRUM (68609-575-55)

NDC Record

Field Name Field Value Definition
PRODUCT NDC68609-575The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMESani-Foam Instant Hand SanitizerThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/31/2004This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEGeneral Products & Supply, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023