NDC 72667-017 Hashtagsun Spf 50 Sunscreen Dabber

Avobenzone, Humosalate, Octisalate, Octocrylene

NDC Product Code 72667-017

NDC CODE: 72667-017

Proprietary Name: Hashtagsun Spf 50 Sunscreen Dabber 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, Humosalate, 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

  • 72667 - Inspec Solutions
    • 72667-017 - Hashtagsun Spf 50 Sunscreen Dabber

NDC 72667-017-01

Package Description: 19 mL in 1 BOTTLE, PLASTIC

NDC Product Information

Hashtagsun Spf 50 Sunscreen Dabber with NDC 72667-017 is a a human over the counter drug product labeled by Inspec Solutions. The generic name of Hashtagsun Spf 50 Sunscreen Dabber is avobenzone, humosalate, octisalate, octocrylene. The product's dosage form is sponge and is administered via topical form.

Labeler Name: Inspec Solutions

Dosage Form: Sponge - A porous, interlacing, absorbent material that contains a drug. It is typically used for applying or introducing medication, or for cleansing. A sponge usually retains its shape.

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.

Hashtagsun Spf 50 Sunscreen Dabber 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.

  • HOMOSALATE 15 g/100mL
  • OCTOCRYLENE 10 g/100mL
  • AVOBENZONE 3 g/100mL
  • OCTISALATE 5 g/100mL

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: Inspec Solutions
Labeler Code: 72667
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: 01-29-2021 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 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Hashtagsun Spf 50 Sunscreen Dabber Product Label Images

Hashtagsun Spf 50 Sunscreen Dabber 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

Otc - Active Ingredient

Active ingredientAvobenzone 3.0% Homosalate 15% Octisalate 5% Octocrylene 10%

Otc - When Using

When using this product:• keep out of eyes. Rinse with water to remove.• Keep away from face to avoid breathing it.• Do not puncture or incinerate, Contents under pressure• Do not store at temperature above 120⁰FStop use and ask a doctor if rash occurs.

• keep out of eyes. Rinse with water to remove.• Keep away from face to avoid breathing it.• Do not puncture or incinerate, Contents under pressure• Do not store at temperature above 120⁰FStop use and ask a doctor if rash occurs.

Otc - Purpose

Avobenzone 3.0% ……………………………………………………………………………… SunscreenHomosalate 15.0% ……………………………………………………………………………. SunscreenOctisalate 5.0% …………………………………………………………………………………. SunscreenOctocrylene 10.0% ……………………………………………………………………………. Sunscreen

Otc - Stop Use

Stop use and ask a doctor if rash occurs.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Inactive Ingredient

Behenyl AlcoholBHTButyloctyl SalicylateCaprylyl Methicone DimethiconeDimethyl CapramideDisodium EDTAEthylhexyl StearateEthylhexylglycerinFragranceGlyceryl Stearate Hydrated SilicaPEG-100 StearatePhenoxyethanolPolyester-8Sodium PolyacrylateStyrene/Acrylates CopolymerTrideceth-6TrimethylsiloxysilicateVP/Hexadecene CopolymerWaterXanthan Gum

* Please review the disclaimer below.