74164-002 NDC - LILY HAND SANITIZER GEL ()

Drug Information

Product NDC: 74164-002

Proprietary Name: Lily Hand Sanitizer Gel

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: My Hao
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:4/13/2020

Package Information

No. Package Code Package Description Billing Unit
174164-002-0330 mL in 1 BOTTLE, DISPENSING (74164-002-03)
274164-002-0660 mL in 1 BOTTLE, DISPENSING (74164-002-06)
374164-002-101000 mL in 1 BOTTLE, DISPENSING (74164-002-10)
474164-002-113785 mL in 1 BOTTLE, DISPENSING (74164-002-11)
574164-002-222000 mL in 1 BOTTLE, DISPENSING (74164-002-22)
674164-002-333000 mL in 1 BOTTLE, DISPENSING (74164-002-33)
774164-002-444000 mL in 1 BOTTLE, DISPENSING (74164-002-44)
874164-002-551890 mL in 1 BOTTLE, DISPENSING (74164-002-55)
974164-002-565678 mL in 1 BOTTLE, DISPENSING (74164-002-56)

NDC Record

Field Name Field Value Definition
PRODUCT NDC74164-002The 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 NAMELily Hand Sanitizer GelThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE7/23/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEMy HaoName of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC74164-002The 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 NAMELily Hand Sanitizer GelThe 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 NAMEMy HaoName 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