NDC 70604-050 Daily Beauty Regimen With Trihex Technology

Titanium Dioxide And Zinc Oxide Kit - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
Proprietary Name:
Daily Beauty Regimen With Trihex Technology
Non-Proprietary Name: [1]
Titanium Dioxide And Zinc Oxide
NDC Directory Status:
Human Otc Drug
Product Type: [3]
Dosage Form:
Kit - A packaged collection of related material.
Labeler Code:
FDA Application Number: [6]
Marketing Category: [8]
Start Marketing Date: [9]
Listing Expiration Date: [11]
Exclude Flag: [12]
Code Navigator:

Product Characteristics

BROWN (C48332)

Code Structure Chart

Product Details

What is NDC 70604-050?

The NDC code 70604-050 is assigned by the FDA to the product Daily Beauty Regimen With Trihex Technology which is a human over the counter drug product labeled by Alastin Skincare, Inc.. The generic name of Daily Beauty Regimen With Trihex Technology is titanium dioxide and zinc oxide. The product's dosage form is kit. The product is distributed in a single package with assigned NDC code 70604-050-00 1 kit in 1 carton * 53.2 ml in 1 bottle, plastic * 14.8 ml in 1 bottle, pump * 29.6 ml in 1 tube * 12 g in 1 tube (70604-011-00). 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 Daily Beauty Regimen With Trihex Technology?

Apply liberally 15 minutes before sun exposureReapply:After 40 minutes of swimming or sweatingImmediately after towel dryingAt least every 2 hoursChildren under 6 months of age: Ask a doctor.Sun Protection measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:Limit time in the sun, especially from 10am - 2pmWear long-sleeved shirts, pants, hats and sunglasses.

Which are Daily Beauty Regimen With Trihex Technology UNII Codes?

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

Which are Daily Beauty Regimen With Trihex Technology 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".