NDC 79596-005 Too Faced Hangover Good To Go Spf 25 Broad Spectrum Moisturizer

Avobenzone, Homosalate, Octisalate, And Octocrylene

NDC Product Code 79596-005

NDC Code: 79596-005

Proprietary Name: Too Faced Hangover Good To Go Spf 25 Broad Spectrum Moisturizer 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, And 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

  • 79596 - Too Faced Cosmetics Llc
    • 79596-005 - Too Faced Hangover Good To Go Spf 25 Broad Spectrum Moisturizer

NDC 79596-005-01

Package Description: 1 TUBE in 1 CARTON > 40 mL in 1 TUBE

NDC Product Information

Too Faced Hangover Good To Go Spf 25 Broad Spectrum Moisturizer with NDC 79596-005 is a a human over the counter drug product labeled by Too Faced Cosmetics Llc. The generic name of Too Faced Hangover Good To Go Spf 25 Broad Spectrum Moisturizer is avobenzone, homosalate, octisalate, and octocrylene. The product's dosage form is lotion and is administered via topical form.

Labeler Name: Too Faced Cosmetics Llc

Dosage Form: Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2

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.

Too Faced Hangover Good To Go Spf 25 Broad Spectrum Moisturizer 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.

  • AVOBENZONE .0306 g/mL
  • HOMOSALATE .0816 g/mL
  • OCTISALATE .051 g/mL
  • OCTOCRYLENE .0816 g/mL

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.

  • WATER (UNII: 059QF0KO0R)
  • ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
  • PEG-100 STEARATE (UNII: YD01N1999R)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • HYALURONATE SODIUM (UNII: YSE9PPT4TH)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • CINNAMON BARK OIL (UNII: XE54U569EC)
  • JOJOBA OIL (UNII: 724GKU717M)
  • SODIUM ACETATE (UNII: 4550K0SC9B)
  • ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
  • INULIN (UNII: JOS53KRJ01)
  • LACTOBACILLUS REUTERI (UNII: 9913I24QEE)
  • OCTYLDODECANOL (UNII: 461N1O614Y)
  • SARCOSINE (UNII: Z711V88R5F)
  • POWDERED CELLULOSE (UNII: SMD1X3XO9M)
  • CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
  • CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ)
  • STEARETH-20 (UNII: L0Q8IK9E08)
  • HEXYLENE GLYCOL (UNII: KEH0A3F75J)
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • SODIUM HYDROXIDE (UNII: 55X04QC32I)
  • COCONUT WATER (UNII: 267F5Y81NT)
  • EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
  • TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
  • SODIUM BENZOATE (UNII: OJ245FE5EU)

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: Too Faced Cosmetics Llc
Labeler Code: 79596
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: 06-15-2019 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: 12-31-2020 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’.

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Too Faced Hangover Good To Go Spf 25 Broad Spectrum Moisturizer Product Label Images

Too Faced Hangover Good To Go Spf 25 Broad Spectrum Moisturizer 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

Other

Drug Facts

Active Ingredient

Avobenzone 3%Homosalate 8%Octisalate 5%Octocrylene 8%

Purpose

Sunscreen

Use

Helps prevent sunburn

Warnings

For external use only

Otc - Do Not Use

Do not use on damaged or broken skin

Otc - When Using

When using this product keep out of eyes. Rinse with water to remove.

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

Directions

  • For sunscreen use:apply generously and evenly 15 minutes before sun exposurereapply at least every two 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 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 sunglasseschildren under 6 months of age: ask a doctor

Inactive Ingredients

Water\Aqua\Eau, C12-15 Alkyl Benzoate, Glycerin, Octyldodecyl Neopentanoate, Butylene Glycol, Glyceryl Stearate, PEG-100 Stearate, Tocopheryl Acetate, Sodium Hyaluronate, Aloe Barbadensis Leaf Extract, Cinnamomum Zeylanicum Bark Extract, Simmondsia Chinensis (Jojoba) Seed Oil, Sodium Acetate, Beeswax\Cera Alba\Cire D'abeille, Ethylhexylglycerin, Inulin, Lactobacillus Ferment, Octyldodecanol, Sarcosine, Yogurt Powder, Cellulose, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Capryloyl Glycine, Steareth-20, Hydroxyethylcellulose, Hexylene Glycol, Citric Acid, Sodium Hydroxide, Fragrance (Parfum), Cocos Nucifera (Coconut) Water, Disodium EDTA, Tetrahexyldecyl Ascorbate, Phenoxyethanol, Potassium Sorbate, Sodium Benzoate

Other Information

Protect the product in this container from excessive heat and direct sun

Questions?

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