90116-547 NDC - HAND SANTIZER ()

Drug Information

Product NDC: 90116-547

Proprietary Name: Hand Santizer

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Smart Solutions, Inc
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:8/10/2020

Package Information

No. Package Code Package Description Billing Unit
190116-547-013785 mL in 1 JUG (90116-547-01)
290116-547-0259 mL in 1 BOTTLE (90116-547-02)
390116-547-04118 mL in 1 BOTTLE (90116-547-04)
490116-547-0518927 mL in 1 PAIL (90116-547-05)
590116-547-08237 mL in 1 BOTTLE (90116-547-08)
690116-547-16473 mL in 1 BOTTLE (90116-547-16)
790116-547-32946 mL in 1 BOTTLE (90116-547-32)
890116-547-331249186 mL in 1 CONTAINER (90116-547-33)
990116-547-55208198 mL in 1 DRUM (90116-547-55)

NDC Record

Field Name Field Value Definition
PRODUCT NDC90116-547The 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 SantizerThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE8/10/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMESmart Solutions, IncName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 4/12/2024