79637-120 NDC - SANASKIN HAND AND BODY SANITIZER ()

Drug Information

Product NDC: 79637-120

Proprietary Name: SanaSkin Hand and Body Sanitizer

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Sanitin Products, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:7/21/2020

Package Information

No. Package Code Package Description Billing Unit
179637-120-0150 mL in 1 BOTTLE, PUMP (79637-120-01)
279637-120-02100 mL in 1 BOTTLE, PUMP (79637-120-02)
379637-120-0320 mL in 1 BOTTLE, SPRAY (79637-120-03)
479637-120-04120 mL in 1 BOTTLE, SPRAY (79637-120-04)
579637-120-08240 mL in 1 BOTTLE, SPRAY (79637-120-08)
679637-120-401000 mL in 1 BOTTLE, PLASTIC (79637-120-40)
779637-120-411000 mL in 1 BOTTLE, SPRAY (79637-120-41)
879637-120-503740 mL in 1 JUG (79637-120-50)
979637-120-70208000 mL in 1 DRUM (79637-120-70)
1079637-120-801054000 mL in 1 CONTAINER (79637-120-80)

NDC Record

Field Name Field Value Definition
PRODUCT NDC79637-120The 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 NAMESanaSkin Hand and Body 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 DATE7/21/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMESanitin Products, LLCName 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