21695-642 NDC - FLEXALL PAIN RELIEVING ()

Drug Information

Product NDC: 21695-642

Proprietary Name: Flexall Pain Relieving

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Rebel Distributors Corp
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:1/1/1997

Package Information

No. Package Code Package Description Billing Unit
121695-642-031 TUBE in 1 CARTON (21695-642-03) / 85 g in 1 TUBEGM

NDC Record

Field Name Field Value Definition
PRODUCT NDC21695-642The 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 NAMEFlexall Pain RelievingThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/1/1997This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMERebel Distributors CorpName 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