75132-012 NDC - FOAM HAND SANITIZER ()

Drug Information

Product NDC: 75132-012

Proprietary Name: Foam Hand Sanitizer

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Guangdong Kemei Pharmaceutical Technology Co., Ltd.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:4/12/2020

Package Information

No. Package Code Package Description Billing Unit
175132-012-013785 mL in 1 BOTTLE (75132-012-01)
275132-012-02950 mL in 1 BOTTLE (75132-012-02)
375132-012-03950 mL in 1 BAG (75132-012-03)

NDC Record

Field Name Field Value Definition
PRODUCT NDC75132-012The 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 NAMEFoam 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 DATE4/12/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEGuangdong Kemei Pharmaceutical Technology Co., Ltd.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