77998-001 NDC - EMELY HAND SANITIZER ()

Drug Information

Product NDC: 77998-001

Proprietary Name: Emely Hand Sanitizer

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Laboratorios E&M SRL
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:6/1/2020

Package Information

No. Package Code Package Description Billing Unit
177998-001-1060 mL in 1 BOTTLE, PLASTIC (77998-001-10)
277998-001-20120 mL in 1 BOTTLE, PLASTIC (77998-001-20)
377998-001-30240 mL in 1 BOTTLE, PLASTIC (77998-001-30)
477998-001-40480 mL in 1 BOTTLE, PLASTIC (77998-001-40)
577998-001-50960 mL in 1 BOTTLE, PLASTIC (77998-001-50)
677998-001-601920 mL in 1 BOTTLE, PLASTIC (77998-001-60)
777998-001-703785 mL in 1 BOTTLE, PLASTIC (77998-001-70)

NDC Record

Field Name Field Value Definition
PRODUCT NDC77998-001The 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 NAMEEmely 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 DATE6/1/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMELaboratorios E&M SRLName 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