74220-003 NDC - HAND SANITIZER ()

Drug Information

Product NDC: 74220-003

Proprietary Name: Hand Sanitizer

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Super Dope Laboratories LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/30/2020

Package Information

No. Package Code Package Description Billing Unit
174220-003-0160 mL in 1 BOTTLE (74220-003-01)
274220-003-02100 mL in 1 BOTTLE (74220-003-02)
374220-003-03120 mL in 1 BOTTLE (74220-003-03)
474220-003-04500 mL in 1 BOTTLE (74220-003-04)
574220-003-05750 mL in 1 BOTTLE (74220-003-05)
674220-003-061000 mL in 1 BOTTLE (74220-003-06)
774220-003-083790 mL in 1 BOTTLE (74220-003-08)
874220-003-091419528.75 mL in 1 DRUM (74220-003-09)
974220-003-10355 mL in 1 BOTTLE (74220-003-10)
1074220-003-11237 mL in 1 BOTTLE (74220-003-11)
1174220-003-17100 PACKET in 1 BOX (74220-003-17) / 2 mL in 1 PACKET (74220-003-07)

NDC Record

Field Name Field Value Definition
PRODUCT NDC74220-003The 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 DATE3/30/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMESuper Dope Laboratories 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