74928-002 NDC - HAND SANITIZER ()

Drug Information

Product NDC: 74928-002

Proprietary Name: HAND SANITIZER

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Shantou Wanli Biotechnology Co.,Ltd.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:4/13/2020

Package Information

No. Package Code Package Description Billing Unit
174928-002-0130 mL in 1 BOTTLE (74928-002-01)
274928-002-0260 mL in 1 BOTTLE (74928-002-02)
374928-002-03100 mL in 1 BOTTLE (74928-002-03)
474928-002-04200 mL in 1 BOTTLE (74928-002-04)
574928-002-05250 mL in 1 BOTTLE (74928-002-05)
674928-002-06500 mL in 1 BOTTLE (74928-002-06)
774928-002-07750 mL in 1 BOTTLE (74928-002-07)
874928-002-081000 mL in 1 BOTTLE (74928-002-08)

NDC Record

Field Name Field Value Definition
PRODUCT NDC74928-002The 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 DATE4/13/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEShantou Wanli Biotechnology 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