72128-001 NDC - REVLEX ARTHRITIS PAIN RELIEF ()

Drug Information

Product NDC: 72128-001

Proprietary Name: Revlex Arthritis Pain Relief

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Cura Health Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/1/2018

Package Information

No. Package Code Package Description Billing Unit
172128-001-151 BOTTLE, WITH APPLICATOR in 1 BOX (72128-001-15) / 15 mL in 1 BOTTLE, WITH APPLICATOR
272128-001-451 BOTTLE, WITH APPLICATOR in 1 BOX (72128-001-45) / 45 mL in 1 BOTTLE, WITH APPLICATOR

NDC Record

Field Name Field Value Definition
PRODUCT NDC72128-001The 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 NAMERevlex Arthritis Pain ReliefThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/1/2018This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMECura Health 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