79384-101 NDC - CONTAMINX ()

Drug Information

Product NDC: 79384-101

Proprietary Name: ContaminX

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Spotlight Medical Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:8/7/2020

Package Information

No. Package Code Package Description Billing Unit
179384-101-0159 mL in 1 BOTTLE, PLASTIC (79384-101-01)
279384-101-0288 mL in 1 BOTTLE, PLASTIC (79384-101-02)
379384-101-03118 mL in 1 BOTTLE, PLASTIC (79384-101-03)
479384-101-04236 mL in 1 BOTTLE, PLASTIC (79384-101-04)
579384-101-05354 mL in 1 BOTTLE, PLASTIC (79384-101-05)
679384-101-06473 mL in 1 BOTTLE, PLASTIC (79384-101-06)
779384-101-081892 mL in 1 BOTTLE, PLASTIC (79384-101-08)
879384-101-109465 mL in 1 BOTTLE, PLASTIC (79384-101-10)
979384-101-1118927 mL in 1 BOTTLE, PLASTIC (79384-101-11)

NDC Record

Field Name Field Value Definition
PRODUCT NDC79384-101The 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 NAMEContaminXThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE8/7/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMESpotlight Medical 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