77283-001 NDC - ONKOHEALTH HAND AND SURFACE SANITIZER ()

Drug Information

Product NDC: 77283-001

Proprietary Name: OnkoHealth Hand and surface sanitizer

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	ONKO PHARMACEUTICALS USA INC.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	5/11/2020

No.	Package Code	Package Description
1	77283-001-01	100 mL in 1 BOTTLE, PLASTIC (77283-001-01)
2	77283-001-02	150 mL in 1 BOTTLE, PLASTIC (77283-001-02)
3	77283-001-03	236 mL in 1 BOTTLE, PLASTIC (77283-001-03)
4	77283-001-04	473 mL in 1 BOTTLE, PLASTIC (77283-001-04)
5	77283-001-05	1000 mL in 1 BOTTLE, PLASTIC (77283-001-05)
6	77283-001-06	3790 mL in 1 BOTTLE, PLASTIC (77283-001-06)
7	77283-001-07	10000 mL in 1 BOTTLE, PLASTIC (77283-001-07)
8	77283-001-08	20000 mL in 1 BOTTLE, PLASTIC (77283-001-08)
9	77283-001-09	355 mL in 1 BOTTLE, PLASTIC (77283-001-09)

Field Name	Field Value	Definition
PRODUCT NDC	77283-001	The 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 NAME	OnkoHealth Hand and surface sanitizer	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	5/11/2020	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	ONKO PHARMACEUTICALS USA INC.	Name 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