69423-568 NDC - HEAD AND SHOULDERS CLINICAL DANDRUFF DEFENSE DRY SCALP RESCUE ()

Drug Information

Product NDC: 69423-568

Proprietary Name: Head and Shoulders Clinical Dandruff Defense Dry Scalp Rescue

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: The Procter & Gamble Manufacturing Company
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:1/11/2021

Package Information

No. Package Code Package Description Billing Unit
169423-568-27270 mL in 1 TUBE (69423-568-27)

NDC Record

Field Name Field Value Definition
PRODUCT NDC69423-568The 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 NAMEHead and Shoulders Clinical Dandruff Defense Dry Scalp RescueThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/11/2021This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEThe Procter & Gamble Manufacturing CompanyName 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