71120-112 NDC - HAND SANITIZER ()

Drug Information

Product NDC: 71120-112

Proprietary Name: Hand Sanitizer

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Sanit Technologies LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:10/6/2020

Package Information

No. Package Code Package Description Billing Unit
171120-112-0118 mL in 1 CONTAINER (71120-112-01)
271120-112-0224 CONTAINER in 1 PACKAGE (71120-112-02) / 18 mL in 1 CONTAINER
371120-112-0348 CONTAINER in 1 PACKAGE (71120-112-03) / 18 mL in 1 CONTAINER
471120-112-0450 mL in 1 CONTAINER (71120-112-04)
571120-112-051000 mL in 1 CONTAINER (71120-112-05)
671120-112-06550 mL in 1 CONTAINER (71120-112-06)
771120-112-07250 mL in 1 CONTAINER (71120-112-07)
871120-112-08300 mL in 1 CONTAINER (71120-112-08)
971120-112-093785 mL in 1 CONTAINER (71120-112-09)
1071120-112-10118 mL in 1 BOTTLE, SPRAY (71120-112-10)
1171120-112-11236 mL in 1 BOTTLE, SPRAY (71120-112-11)

NDC Record

Field Name Field Value Definition
PRODUCT NDC71120-112The 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 NAMEHand 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 DATE10/6/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMESanit Technologies 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