28851-695 NDC - KENDALL SOOTHING ()

Drug Information

Product NDC: 28851-695

Proprietary Name: Kendall Soothing

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Covidien Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:4/22/2011

Package Information

No. Package Code Package Description Billing Unit
128851-695-0159 mL in 1 TUBE (28851-695-01)ML
228851-695-02118 mL in 1 TUBE (28851-695-02)ML
328851-695-034 mL in 1 POUCH (28851-695-03)ML

NDC Record

Field Name Field Value Definition
PRODUCT NDC28851-695The 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 NAMEKendall SoothingThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE4/22/2011This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMECovidien 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