Spf Bestsellers Starter Kit
Avobenzone, Homosalate, Octisalate, Octocrylene
Supergoop, Llc
Human Otc Drug
NDC 75936-410Spf Bestsellers Starter Kit also known as Avobenzone, Homosalate, Octisalate, Octocrylene is a human otc drug labeled by 'Supergoop, Llc'. National Drug Code (NDC) number for Spf Bestsellers Starter Kit is 75936-410. This drug is available in dosage form of Kit. The names of the active, medicinal ingredients in Spf Bestsellers Starter Kit drug includes . The currest status of Spf Bestsellers Starter Kit drug is Active.
Drug Information:
| Drug NDC: | 75936-410 |
| The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC. |
| Proprietary Name: | Spf Bestsellers Starter Kit |
| Also known as the trade name. It is the name of the product chosen by the labeler. |
| Product Type: | Human Otc Drug |
| Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing. |
| Non Proprietary Name: | Avobenzone, Homosalate, Octisalate, Octocrylene |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Supergoop, Llc |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Kit |
| The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources. |
| Status: | Active |
| FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved. |
| Substance Name: | |
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. |
| Route Details: | |
| The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. |
Marketing Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Marketing Category: | OTC MONOGRAPH FINAL |
| Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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. |
| Marketing Start Date: | 24 Sep, 2021 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 14 Jun, 2026 |
| This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached. |
| Application Number: | part352 |
| 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. |
| Listing Expiration Date: | 31 Dec, 2023 |
| This is the date when the listing record will expire if not updated or certified by the firm. |
OpenFDA Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Manufacturer Name: | Supergoop, LLC
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| Original Packager: | Yes
|
| Whether or not the drug has been repackaged for distribution. |
| UPC: | 0816218028886
|
| UPC stands for Universal Product Code. |
| UNII: | |
| Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information. |
Packaging Information:
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|
| 75936-410-01 | 1 KIT in 1 KIT (75936-410-01) * 15 mL in 1 TUBE (75936-411-01) * 30 mL in 1 BOTTLE (75936-413-01) * 15 mL in 1 BOTTLE (75936-412-01) | 24 Sep, 2021 | N/A | No |
| Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together. |
Purpose:
Uses helps prevent sunburn if used as directed with other sun protection measures (see directions), decreases the risk of skin cancer and early skin aging caused by the sun
Product Elements:
Spf bestsellers starter kit avobenzone, homosalate, octisalate, octocrylene glowscreen spf40 avobenzone, octisalate, octocrylene niacinamide ethylhexyl hydroxystearate butylene glycol hydroxyacetophenone caprylyl glycol medium-chain triglycerides limonium gerberi whole leuconostoc/radish root ferment filtrate pantothenic acid tocopherol sunflower oil isododecane arginine cetyl phosphate coco-caprylate 1,2-hexanediol water butyloctyl salicylate isodecyl neopentanoate glyceryl monostearate cocoa propanediol alkyl (c12-15) benzoate polymethylsilsesquioxane (4.5 microns) ferulic acid diisopropyl sebacate trisodium ethylenediamine disuccinate glycerin glyceryl stearate citrate bismuth oxychloride mica titanium dioxide lauryl lactate chlorphenesin hyaluronate sodium ferric oxide red carbomer interpolymer type a (allyl sucrose crosslinked) avobenzone avobenzone octisalate octisalate octocrylene octocrylene unseen sunscreen broad spectrum spf 40 avobenzone, homosalate, octocrylene, octisalate polyester-7 neopentyl glycol diheptanoate zinc sulfate tocopherol phymatolithon calcareum shea butter indian frankincense diatomaceous earth dicaprylyl carbonate medium-chain triglycerides mannitol polymethylsilsesquioxane (11 microns) isohexadecane microcrystalline cellulose silicon dioxide lecithin, sunflower dimethicone crosspolymer (450000 mpa.s at 12% in cyclopentasiloxane) dimethicone/bis-isobutyl ppg-20 crosspolymer isododecane homosalate homosalate avobenzone avobenzone octocrylene octocrylene octisalate octisalate play everyday spf 50 with sunflower extract avobenzone, homosalate, octisalate, octocrylene isododecane water diisopropyl sebacate glycerin isodecyl neopentanoate lauryl lactate homosalate homosalate octisalate octisalate octocrylene octocrylene avobenzone avobenzone
Indications and Usage:
Stop use and ask a doctor if rash occurs.
Warnings:
For external use only do not use on damaged or broken skin when using this product, keep out of eyes. rinse with water to remove
Dosage and Administration:
Unseen sunscreen spf 40 directions directions apply generously and evenly 15 minutes before sun exposure reapply: after 40 minutes of swimming or sweating immediately after towel drying at least every 2 hours 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 10 a.m.-2 p.m. wear long-sleeved shirts, pants, hats, and sunglasses children under 6 months: ask a doctor
Glowscreen spf 40 directions directions apply generously and evenly 15 minutes before sun exposure reapply at least every 2 hours use a water resistant sunscreen if swimming or sweating 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 10a.m. â 2p.m. wear long-sleeved shirts, pants, hats, and sunglasses children under 6 months: ask a doctor
Play everyday sunscreen spf 50 with sunflower extract directions directions apply liberally 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 increases your risk of skin cancer and early skin aging. to decrease this risk, regularly use a sunscreen with broad spectrum spf 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
Package Label Principal Display Panel:
Spf bestsellers starter kit spf bestsellers starter kit discover healthier, happier skin with bestselling spf for face & body. unseen sunscreen spf 40 0.5 fl. oz. / 15 ml glowscreen spf 40 0.5fl. oz. / 15 ml play everyday lotion spf 50 with sunflower extract 1 fl. oz. / 30 ml kit front kit back