NDC 69840-020 Yes To Booty-ful Paper Mask - Detoxified Plus Acne-free

Salicylic Acid

NDC Product Code 69840-020

NDC Code: 69840-020

Proprietary Name: Yes To Booty-ful Paper Mask - Detoxified Plus Acne-free 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: Salicylic Acid 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

  • 69840 - Yes To, Inc.
    • 69840-020 - Yes To Booty-ful Paper Mask - Detoxified Plus Acne-free

NDC 69840-020-11

Package Description: 2 PATCH in 1 PACKET > 10 mL in 1 PATCH

NDC Product Information

Yes To Booty-ful Paper Mask - Detoxified Plus Acne-free with NDC 69840-020 is a a human over the counter drug product labeled by Yes To, Inc.. The generic name of Yes To Booty-ful Paper Mask - Detoxified Plus Acne-free is salicylic acid. The product's dosage form is cloth and is administered via topical form.

Labeler Name: Yes To, Inc.

Dosage Form: Cloth - A large piece of relatively flat, absorbent material that contains a drug. It is typically used for applying medication or for cleansing.

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.

Yes To Booty-ful Paper Mask - Detoxified Plus Acne-free 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.

  • SALICYLIC ACID 5 mg/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.

  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • WATER (UNII: 059QF0KO0R)
  • HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)
  • PROPANEDIOL (UNII: 5965N8W85T)
  • ALLANTOIN (UNII: 344S277G0Z)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)
  • SOLANUM LYCOPERSICUM (UNII: 0243Q4990L)
  • MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)
  • SORBITOL (UNII: 506T60A25R)
  • TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
  • ENOXOLONE DIPOTASSIUM (UNII: ZJI2YIM6Z9)
  • XANTHAN GUM (UNII: TTV12P4NEE)
  • CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
  • GELLAN GUM (LOW ACYL) (UNII: 7593U09I4D)
  • SALIX ALBA BARK (UNII: 205MXS71H7)
  • GINKGO (UNII: 19FUJ2C58T)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • PUMPKIN (UNII: SYW0QUB89Y)
  • MATRICARIA CHAMOMILLA LEAF (UNII: 6I9LN466F0)
  • ASPALATHUS LINEARIS LEAF (UNII: H7UGK1GJCU)
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • SODIUM HYDROXIDE (UNII: 55X04QC32I)
  • 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
  • SODIUM BENZOATE (UNII: OJ245FE5EU)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
  • ALCOHOL (UNII: 3K9958V90M)

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: Yes To, Inc.
Labeler Code: 69840
FDA Application Number: part333D 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 FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph. 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: 06-01-2019 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’.

* Please review the disclaimer below.

Yes To Booty-ful Paper Mask - Detoxified Plus Acne-free Product Label Images

Yes To Booty-ful Paper Mask - Detoxified Plus Acne-free 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

Salicylic Acid 0.5%

Purpose

Acne Treatment

Use

For the treatment of acne

Warnings

For external use only

When Using This Product

  • Skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.Avoid contact with the eyes.

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.

Questions?

Visit yesto.com

Directions

  • Clean the skin thoroughly before applying this productunfold and adjust the mask to cover the entire affected area, one time daily for 10 minutes, then remove and disposebecause excessive drying of the skin may occur, start with one application daily or as directed by a doctorif bothersome dryness or peeling occurs, reduce usage to every other day.

Inactive Ingredients

Water (Aqua), Aloe Barbadensis Leaf Juice, SD Alcohol 40-B, Propanediol. Hamamelis Virginiana (Witch Hazel) Water, Glycerin, Sorbitol, Solanum Lycopersicum (Tomato) Fruit Extract, Charcoal Powder, Salix Alba (Willow) Bark Extract, Cucurbita Pepo (Pumpkin) Fruit Extract, Ginkgo Biloba Leaf Extract, Chamomilla Recutita (Matricaria) Extract, Melaleuca Alternifolia (Tea Tree) Flower/Leaf/Stem Extract, Aspalathus Linearis Extract, Alcohol, Tetrasodium Glutamate Diacetate, Xanthan Gum, Allantoin, 1,2-Hexanediol, Dipotassium Glycyrrhizate, Caprylhydroxamic Acid, Gellan Gum, Sodium Hydroxide, Citric Acid, Sodium Benzoate, Potassium Sorbate, Phenoxyethanol, Fragrance (Parfum), Benzyl Benzoate, Coumarin, Butylphenyl Methylpropional.

* Please review the disclaimer below.

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