71315-100 NDC - APLAUS HAND AND SKIN SANITIZER ()

Drug Information

Product NDC: 71315-100

Proprietary Name: Aplaus Hand and Skin Sanitizer

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Katan Technologies USA, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/1/2017

Package Information

No. Package Code Package Description Billing Unit
171315-100-0110 mL in 1 BOTTLE, SPRAY (71315-100-01)
271315-100-0880 mL in 1 BOTTLE, SPRAY (71315-100-08)
371315-100-22220 mL in 1 BOTTLE, SPRAY (71315-100-22)
471315-100-383780 mL in 1 JUG (71315-100-38)
571315-100-5050 mL in 1 BOTTLE, SPRAY (71315-100-50)
671315-100-55550 mL in 1 BOTTLE, PUMP (71315-100-55)
771315-100-6060 mL in 1 BOTTLE, SPRAY (71315-100-60)
871315-100-991000 mL in 1 BOTTLE, SPRAY (71315-100-99)

NDC Record

Field Name Field Value Definition
PRODUCT NDC71315-100The 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 NAMEAplaus Hand and Skin 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 DATE5/1/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEKatan Technologies USA, LLCName 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