NDC 73291-0005 Sunbetter Broad Spectrum Spf 56 Sunscreen Compact Sheer

Zinc Oxide,Titanium Dioxide Stick Topical - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
73291-0005
Proprietary Name:
Sunbetter Broad Spectrum Spf 56 Sunscreen Compact Sheer
Non-Proprietary Name: [1]
Zinc Oxide, Titanium Dioxide
Substance Name: [2]
Titanium Dioxide; Zinc Oxide
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Stick - A dosage form prepared in a relatively long and slender often cylindrical form.
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]
    Skinbetter Science Llc
    Labeler Code:
    73291
    FDA Application Number: [6]
    M020
    Marketing Category: [8]
    OTC MONOGRAPH DRUG -
    Start Marketing Date: [9]
    02-01-2021
    Listing Expiration Date: [11]
    12-31-2025
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 73291-0005-1

    Package Description: 12 g in 1 CONTAINER

    Product Details

    What is NDC 73291-0005?

    The NDC code 73291-0005 is assigned by the FDA to the product Sunbetter Broad Spectrum Spf 56 Sunscreen Compact Sheer which is a human over the counter drug product labeled by Skinbetter Science Llc. The generic name of Sunbetter Broad Spectrum Spf 56 Sunscreen Compact Sheer is zinc oxide, titanium dioxide. The product's dosage form is stick and is administered via topical form. The product is distributed in a single package with assigned NDC code 73291-0005-1 12 g in 1 container . 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 Sunbetter Broad Spectrum Spf 56 Sunscreen Compact Sheer?

    Apply liberally and evenly 15 minutes before sun exposure.Reapply:after 80 minutes of swimming or sweating.immediately after towel drying.at least every 2 hours.Sun Protection Measures. Spending time in the sun ircreases 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 10 a.m. - 2 p.m.wear long-sleeved shirts, pants, hats, and sunglasses.Children under 6 months: Ask a doctor.

    What are Sunbetter Broad Spectrum Spf 56 Sunscreen Compact Sheer Active Ingredients?

    An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    Which are Sunbetter Broad Spectrum Spf 56 Sunscreen Compact Sheer UNII Codes?

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

    Which are Sunbetter Broad Spectrum Spf 56 Sunscreen Compact Sheer 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.

    [2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    [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 ("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".