75015-000 NDC - HAND SANITIZER ()

Drug Information

Product NDC: 75015-000

Proprietary Name: Hand Sanitizer

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Lubrication Specialties, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:4/9/2020

Package Information

No. Package Code Package Description Billing Unit
175015-000-00118.3 mL in 1 BOTTLE, PLASTIC (75015-000-00)
275015-000-01236.6 mL in 1 BOTTLE, PLASTIC (75015-000-01)
375015-000-02473 mL in 1 BOTTLE, PLASTIC (75015-000-02)
475015-000-03946.4 mL in 1 BOTTLE, PLASTIC (75015-000-03)
575015-000-041892 mL in 1 BOTTLE, PLASTIC (75015-000-04)
675015-000-3118927 mL in 1 PAIL (75015-000-31)
775015-000-323785 mL in 1 JUG (75015-000-32)
875015-000-40208198 mL in 1 DRUM (75015-000-40)
975015-000-501000000 mL in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK (75015-000-50)

NDC Record

Field Name Field Value Definition
PRODUCT NDC75015-000The 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 NAMEHand 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 DATE4/9/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMELubrication Specialties, 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