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NDC 10596-003 Hello Sunday Bestseller Daily Spf Duo

Avobenzone,Homosalate,Octisalate,Octocrylene Kit Topical - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 10596-003?
  4. Hello Sunday Bestseller Daily Spf Duo Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

Get all the details for National Drug Code (NDC) 10596-003 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
10596-003
Proprietary Name:
Hello Sunday Bestseller Daily Spf Duo
Non-Proprietary Name: [1]
Avobenzone, Homosalate, Octisalate, Octocrylene
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.
Administration Route(s): [4]
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Labeler Name: [5]
Kao Usa Inc.
Labeler Code:
10596
Product Label ID:
26cf264b-f68d-5691-e063-6394a90a8ab4
FDA Application Number: [6]
M020
Marketing Category: [8]
OTC MONOGRAPH DRUG -
Start Marketing Date: [9]
11-13-2024
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N
Code Navigator:

Code Structure Chart

Product Details

What is NDC 10596-003?

The NDC code 10596-003 is assigned by the FDA to the product Hello Sunday Bestseller Daily Spf Duo which is a human over the counter drug product labeled by Kao Usa Inc.. The generic name of Hello Sunday Bestseller Daily Spf Duo is avobenzone, homosalate, octisalate, octocrylene. The product's dosage form is kit and is administered via topical form. The product is distributed in a single package with assigned NDC code 10596-003-01 1 kit in 1 carton * 50 ml in 1 bottle * 15 ml in 1 tube. 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 Hello Sunday Bestseller Daily Spf Duo?

THE ONE FOR YOUR LIPSApply generously to lips before sun exposure.Reapply frequentlyDo not swallowSun Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin ageing. 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 10 a.m. – 2 p.m.wear long-sleeved shirts, pants, hats, and sunglassesTHE EVERYDAY ONEApply generously on dry skin (we recommend 5 pumps, enough to cover your face, neck and ears) 15 minutes before sun exposure and as a last step in your skincare routine (before makeup).Reapply at least every 2 hoursUse a water resistant sunscreen if swimming or sweatingSun Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin ageing. 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 10 a.m. – 2 p.m.wear long-sleeved shirts, pants, hats, and sunglassesChildren under 6 months of age: Ask a doctor

Which are Hello Sunday Bestseller Daily Spf Duo UNII Codes?

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

Which are Hello Sunday Bestseller Daily Spf Duo 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.

[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

[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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".