NDC 79950-011 Bondi Sands Broad Spectrum Hydra Uv Protect Spf 70 Sunscreen

Avobenzone, Homosalate, Octisalate, Octocrylene

NDC Product Code 79950-011

NDC CODE: 79950-011

Proprietary Name: Bondi Sands Broad Spectrum Hydra Uv Protect Spf 70 Sunscreen What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Avobenzone, Homosalate, Octisalate, Octocrylene 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.

NDC Code Structure

  • 79950 - Bondi Sands (usa) Inc.
    • 79950-011 - Bondi Sands Broad Spectrum Hydra Uv Protect Spf 70 Sunscreen

NDC 79950-011-01

Package Description: 150 mL in 1 BOTTLE, SPRAY

NDC Product Information

Bondi Sands Broad Spectrum Hydra Uv Protect Spf 70 Sunscreen with NDC 79950-011 is a a human over the counter drug product labeled by Bondi Sands (usa) Inc.. The generic name of Bondi Sands Broad Spectrum Hydra Uv Protect Spf 70 Sunscreen is avobenzone, homosalate, octisalate, octocrylene. The product's dosage form is spray and is administered via topical form.

Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.

Product Type: Human Otc Drug 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.

Bondi Sands Broad Spectrum Hydra Uv Protect Spf 70 Sunscreen Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.


Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
  • WATER (UNII: 059QF0KO0R)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • PEG-15 COCAMINE (UNII: 8L6LB12TSJ)
  • CARRAGEENAN (UNII: 5C69YCD2YJ)
  • YELLOW WAX (UNII: 2ZA36H0S2V)
  • SODIUM HYDROXIDE (UNII: 55X04QC32I)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • PEG-40 STEARATE (UNII: ECU18C66Q7)
  • CAPRYLYL GLYCOL (UNII: 00YIU5438U)
  • ETHYL ACRYLATE/METHACRYLIC ACID/STEARETH-20 METHACRYLATE COPOLYMER (UNII: EPA1872R1N)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

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

Labeler Name: Bondi Sands (usa) Inc.
Labeler Code: 79950
FDA Application Number: part352 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.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. 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.

Start Marketing Date: 08-05-2021 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2022 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.

Exclude Flag: N - NO 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".

* Please review the disclaimer below.

Bondi Sands Broad Spectrum Hydra Uv Protect Spf 70 Sunscreen Product Label Images

Bondi Sands Broad Spectrum Hydra Uv Protect Spf 70 Sunscreen Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients

Avobenzone 3%, Homosalate 15%, Octisalate 5%, Octocrylene 10%

Purpose

Sunscreen

Uses

  • Helps prevent sunburnIf used as directed with other sun protection measures (
  • See Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

Warnings

For external use only

Do Not Use

On damaged or broken skin.

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center right away.

When Using This Product

Keep out of eyes. Rinse with water to remove.

Stop Use And Ask A Doctor

If rash occurs.

Directions

  • Apply liberally 15 minutes before sun exposure.Reapply:after 80 minutes of swimming or sweatingimmediately after towel dryingat least every 2 hoursSun 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 10 a.m.- 2 p.m.Wear long-sleeved shirts, pants, hats, and sunglasses.Children under 6 months: Ask a doctor.

Other Information

  • Protect the product in this container from excessive heat and direct sun.You may report a serious adverse reaction to 888-266-0772; Monday – Friday, 9 am – 5 pm.

Inactive Ingredients

Water, Beeswax, C12-15 Alkyl Benzoate, Silica, PEG-15 Cocamine, Caprylyl Glycol, PEG-40 Stearate, Acrylates/Steareth-20 Methacrylate Copolymer, Caprylhydroxamic Acid, Glycerin, Carbomer, Sodium Hydroxide, Phenoxyethanol, Sodium Carrageenan, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Sodium Chloride.

Questions?

888-266-0772 or visit bondisands.com

Company Information

Made in Australia.Distributed by Bondi Sands USAWilmington, DE 19808bondisands.com

Product Packaging

Bondi sandsThe Australian tanBROAD SPECTRUMHYDRAUV PROTECTSPF 70SUNSCREEN SPRAYVERY WATER RESISTANT 80 MINUTESPLANT BASED HYDRATIONREEF FRIENDLYAustralian Made5.07 FL. OZ. (150mL)

* Please review the disclaimer below.