NDC 31720-952 Clear And Cover Acne Treatment Concealer Clear And Cover Acne Treatment Concealer 2 Linen

Salicylic Acid

NDC Product Information

Clear And Cover Acne Treatment Concealer Clear And Cover Acne Treatment Concealer 2 Linen with NDC 31720-952 is a a human over the counter drug product labeled by S+. The generic name of Clear And Cover Acne Treatment Concealer Clear And Cover Acne Treatment Concealer 2 Linen is salicylic acid. The product's dosage form is cream and is administered via topical form.

Labeler Name: S+

Dosage Form: Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.

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.

Clear And Cover Acne Treatment Concealer Clear And Cover Acne Treatment Concealer 2 Linen 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 20 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.

  • WATER (UNII: 059QF0KO0R)
  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • TRISILOXANE (UNII: 9G1ZW13R0G)
  • KAOLIN (UNII: 24H4NWX5CO)
  • PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
  • BORON NITRIDE (UNII: 2U4T60A6YD)
  • TALC (UNII: 7SEV7J4R1U)
  • DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
  • MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)
  • METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • LEVOMENOL (UNII: 24WE03BX2T)
  • CAPRYLYL GLYCOL (UNII: 00YIU5438U)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
  • TOCOPHEROL (UNII: R0ZB2556P8)
  • CHAMOMILE (UNII: FGL3685T2X)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • ALUMINUM OXIDE (UNII: LMI26O6933)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)

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.
  • 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: S+
Labeler Code: 31720
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: 06-01-2020 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.

Clear And Cover Acne Treatment Concealer Clear And Cover Acne Treatment Concealer 2 Linen Product Label Images

Clear And Cover Acne Treatment Concealer Clear And Cover Acne Treatment Concealer 2 Linen 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 Ingredient

Salicylic Acid 2%

Purpose

Acne Treatment

Use

  • For the treatment of acneclears acne blemisheshelps prevent new acne blemishes

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

Keep Out Of Reach Of Children.

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

Directions

  • Clean the skin thoroughly before applying this productcover the entire affected area with a thin layer one to three times dailybecaused excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three tiems daily if needed or as directed by a doctorIf bothersome dryness or peeling occurs, reduce application to once a day or every other day

Inactive Ingredients

Water (Aqua), Cyclopentasiloxane, Butylene Glycol, Dimethicone, Trisiloxane, Kaolin, Polyisobutene, PEG/PPG-18/18 Dimethicone, Boron Nitride, Talc, Cyclodextrin, Cetyl PEG/PPG-10/1 Dimethicone, Disteardimonium Hectorite, Magnesium Sulfate, Methyl Methacrylate Crosspolymer, Trimethylsiloxysilicate, Phenoxyethanol, Bisabolol, Caprylyl Glycol, Glycerin, Triethoxycaprylylsilane, Tocopherol, Chamomilla Recutita (Matricaria) Flower Extract, Tocopheryl Acetate, Alumina, Silica, Pentaerythrityl Tetra-Di-T-Butyl Hydroxyhydrocinnamate.


May Contain (+/-): Zinc Oxide (CI 77947), Titanium Dioxide (CI 77891), Iron Oxides (CI 77491/CI 77492/CI 77499).

* Please review the disclaimer below.