NDC 84126-003 Royal Oils By Head And Shoulders Scalp Care Dual Pack

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

Product Information

NDC Product Code:
84126-003
Proprietary Name:
Royal Oils By Head And Shoulders Scalp Care Dual Pack
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 Code:
84126
FDA Application Number: [6]
M032
Marketing Category: [8]
OTC MONOGRAPH DRUG -
Start Marketing Date: [9]
05-01-2023
Listing Expiration Date: [11]
12-31-2025
Exclude Flag: [12]
N
Code Navigator:

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Product Details

What is NDC 84126-003?

The NDC code 84126-003 is assigned by the FDA to the product Royal Oils By Head And Shoulders Scalp Care Dual Pack which is a human over the counter drug product labeled by The Procter & Gamble Manufacturing Company. The generic name of Royal Oils By Head And Shoulders Scalp Care Dual Pack is pyrithione zinc. The product's dosage form is kit. The product is distributed in a single package with assigned NDC code 84126-003-01 1 kit in 1 cello pack * 380 ml in 1 bottle, plastic (69423-608-38) * 400 ml in 1 bottle, plastic (69423-571-40). 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 Royal Oils By Head And Shoulders Scalp Care Dual Pack?

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 Royal Oils By Head And Shoulders Scalp Care Dual Pack UNII Codes?

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

Which are Royal Oils By Head And Shoulders Scalp Care Dual Pack 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:

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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".