1. Home
  2. Labeler Index
  3. The Procter & Gamble Manufacturing Company
  4. NDC Product Code: 69423-210 Head And Shoulders Dual Pack Smooth And Silky

NDC 69423-210 Head And Shoulders Dual Pack Smooth And Silky

Pyrithione Zinc Kit - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69423-210?
  4. Head And Shoulders Dual Pack Smooth And Silky Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

NDC Product Code:
69423-210
Proprietary Name:
Head And Shoulders Dual Pack Smooth And Silky
Non-Proprietary Name: [1]
Pyrithione Zinc
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Kit - A packaged collection of related material.
Labeler Name: [5]
The Procter & Gamble Manufacturing Company
Labeler Code:
69423
Product Label ID:
a9500735-c938-0ad5-e053-2995a90afa50
FDA Application Number: [6]
M032
Marketing Category: [8]
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date: [9]
01-15-2020
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
N
Code Navigator:

Code Structure Chart

Product Details

What is NDC 69423-210?

The NDC code 69423-210 is assigned by the FDA to the product Head And Shoulders Dual Pack Smooth And Silky which is a human over the counter drug product labeled by The Procter & Gamble Manufacturing Company. The generic name of Head And Shoulders Dual Pack Smooth And Silky is pyrithione zinc. The product's dosage form is kit. The product is distributed in 2 packages with assigned NDC codes 69423-210-01 1 kit in 1 package, combination * 380 ml in 1 bottle, plastic (37000-094-38) * 315 ml in 1 tube (69423-103-31), 69423-210-02 1 kit in 1 carton * 380 ml in 1 bottle, plastic (37000-094-38) * 315 ml in 1 tube (69423-103-31). This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Head And Shoulders Dual Pack Smooth And Silky?

For best results use at least twice a week or as directed by a doctor. for maximum dandruff control, use every time you shampoo.shake before use.wet hair, massage onto scalp, rinse, repeat if desired. for best results use at least twice a week or as directed by a doctor. apply to wet hair after shampooing by gently massaging into hair and scalp, rinse well.

Which are Head And Shoulders Dual Pack Smooth And Silky UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Head And Shoulders Dual Pack Smooth And Silky Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Head And Shoulders Dual Pack Smooth And Silky?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

* Please review the disclaimer below.

Product Footnotes

[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".