78880-017 NDC - HANDY DOCTOR HAND SANITIZER ()

Drug Information

Product NDC: 78880-017

Proprietary Name: Handy Doctor Hand Sanitizer

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Sauber Co.,Ltd.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:1/15/2021

Package Information

No. Package Code Package Description Billing Unit
178880-017-021 CASE in 1 BLISTER PACK (78880-017-02) / 17 mL in 1 CASE

NDC Record

Field Name Field Value Definition
PRODUCT NDC78880-017The 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 NAMEHandy Doctor 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 DATE1/15/2021This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMESauber 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