75012-057 NDC - KELPURE HAND SANITIZER ()

Drug Information

Product NDC: 75012-057

Proprietary Name: KelPure Hand Sanitizer

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: KELMERICA LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/1/2020

Package Information

No. Package Code Package Description Billing Unit
175012-057-08236.6 mL in 1 BOTTLE, PLASTIC (75012-057-08)
275012-057-16473 mL in 1 BOTTLE, PLASTIC (75012-057-16)
375012-057-283780 mL in 1 BOTTLE, PLASTIC (75012-057-28)
475012-057-55207900 mL in 1 DRUM (75012-057-55)
575012-057-9518900 mL in 1 CONTAINER (75012-057-95)

NDC Record

Field Name Field Value Definition
PRODUCT NDC75012-057The 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 NAMEKelPure 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 DATE5/1/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEKELMERICA LLCName of Company corresponding to the labeler code segment of the Product NDC.

Download Record

Download this NDC record in Text format: Export

Download this NDC record in Excel (CSV) format: Export

Download this NDC record in XML format: Export

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