79408-7001 NDC - MOISTURISING HAND SANITIZER ()

Drug Information

Product NDC: 79408-7001

Proprietary Name: Moisturising Hand Sanitizer

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Oceanic SA
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:7/22/2020

Package Information

No. Package Code Package Description Billing Unit
179408-7001-02 mL in 1 POUCH (79408-7001-0)
279408-7001-21 TUBE in 1 CARTON (79408-7001-2) / 50 mL in 1 TUBE
379408-7001-350 POUCH in 1 CARTON (79408-7001-3) / 2 mL in 1 POUCH
479408-7001-41 BOTTLE in 1 CARTON (79408-7001-4) / 250 mL in 1 BOTTLE
579408-7001-51 TUBE in 1 CARTON (79408-7001-5) / 70 mL in 1 TUBE

NDC Record

Field Name Field Value Definition
PRODUCT NDC79408-7001The 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 NAMEMoisturising 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 DATE7/22/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEOceanic SAName 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