NDC 43479-112 Eradikate Acne Mark Fading

Salicylic Acid

NDC Product Code 43479-112

NDC CODE: 43479-112

Proprietary Name: Eradikate Acne Mark Fading 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • This medication is used on the skin to treat common skin and foot (plantar) warts. Salicylic acid helps cause the wart to gradually peel off. This medication is also used to help remove corns and calluses. This product should not be used on the face or on moles, birthmarks, warts with hair growing from them, or genital/anal warts. Salicylic acid is a keratolytic. It belongs to the same class of drugs as aspirin (salicylates). It works by increasing the amount of moisture in the skin and dissolving the substance that causes the skin cells to stick together. This makes it easier to shed the skin cells. Warts are caused by a virus. Salicylic acid does not affect the virus.

NDC Code Structure

  • 43479 - Kate Somerville Skincare, Llc

NDC 43479-112-51

Package Description: 1 BOTTLE in 1 BOX > 30 mL in 1 BOTTLE

NDC Product Information

Eradikate Acne Mark Fading with NDC 43479-112 is a a human over the counter drug product labeled by Kate Somerville Skincare, Llc. The generic name of Eradikate Acne Mark Fading is salicylic acid. The product's dosage form is gel and is administered via topical form.

Labeler Name: Kate Somerville Skincare, Llc

Dosage Form: Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.

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.

Eradikate Acne Mark Fading 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 2 g/100mL

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)
  • COCONUT ALKANES (UNII: 1E5KJY107T)
  • PENTYLENE GLYCOL (UNII: 50C1307PZG)
  • NIACINAMIDE (UNII: 25X51I8RD4)
  • CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • CETEARYL OLIVATE (UNII: 58B69Q84JO)
  • DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
  • POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
  • SORBITAN OLIVATE (UNII: MDL271E3GR)
  • CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
  • MICROCITRUS AUSTRALIS FRUIT (UNII: 9DNS80T428)
  • LENTIL (UNII: 6O38V6B52O)
  • APPLE (UNII: B423VGH5S9)
  • WATERMELON (UNII: 231473QB6R)
  • EREMOCITRUS GLAUCA FRUIT (UNII: 3R0KMY07TY)
  • SODIUM LACTATE (UNII: TU7HW0W0QT)
  • PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)
  • ADENOSINE (UNII: K72T3FS567)
  • DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
  • 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
  • SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
  • .ALPHA.-GLUCAN OLIGOSACCHARIDE (UNII: S95658MI3W)
  • MALTODEXTRIN (UNII: 7CVR7L4A2D)
  • POLYGLYCERYL-3 CAPRATE (UNII: VZQ347QQ3H)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
  • POLYSORBATE 20 (UNII: 7T1F30V5YH)
  • CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
  • ZINC PIDOLATE (UNII: C32PQ86DH4)
  • THYMOL (UNII: 3J50XA376E)
  • TERPINEOL (UNII: R53Q4ZWC99)
  • HEXYLENE GLYCOL (UNII: KEH0A3F75J)
  • CAPRYLYL GLYCOL (UNII: 00YIU5438U)
  • POLYDEXTROSE (UNII: VH2XOU12IE)
  • ICODEXTRIN (UNII: 2NX48Z0A9G)
  • AMYLOPECTIN, UNSPECIFIED SOURCE (UNII: 4XO4QFV777)
  • LACTOBACILLUS REUTERI (UNII: 9913I24QEE)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)
  • SODIUM BENZOATE (UNII: OJ245FE5EU)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)

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: Kate Somerville Skincare, Llc
Labeler Code: 43479
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: 04-01-2021 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 - NO 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Eradikate Acne Mark Fading Product Label Images

Eradikate Acne Mark Fading 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 Ingredients

SALICYLIC ACID- 2%

Purpose

ACNE TREATMENT

Uses

  • FOR THE TREATMENT OF ACNEHELPS KEEP SKIN CLEAR OF NEW ACNE BLEMISHES

Warnings

  • FOR EXTERNAL USE ONLYWHEN USING THIS PRODUCTSKIN IRRITATION OR DRYNESS IS MORE LIKELY TO OCCUR IF YOU USE ANOTHER TOPICAL ACNE MEDICATIONAT THE SAME TIME. IF IRRITATION OCCURS, ONLY USE ONE TOPICAL ACNE MEDICATION AT A TIME.

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.

Directions

  • AM AND PM. APPLY TO TARGETED AREAS OR ALL OVER A CLEANSED AND DRIED FACE, AVOIDING EYE AREA. ALLOW TO FULLY ABSORB INTO THE SKIN.BECAUSE EXCESSIVE DRYING OF THE SKIN MAKE OCCUR, START WITH ONE APPLICATION DAILY, THEN GRADUALLY INCREASE TO TWO OR THREE TIMES DAILY IF NEEDED OR AS DIRECTED BY A DOCTOR.IF BOTHERSOME DRYNESS OR PEELING OCCURS, REDUCE APPLICATION TO ONCE A DAY OR EVERY OTHER DAY.

Inactive Ingredients

WATER/AQUA/EAU, COCONUT ALKANES, PENTYLENE GLYCOL, NIACINAMIDE, CAPRYLYL METHICONE, GLYCERIN, CETEARYL OLIVATE, POLYSILICONE-11, POTASSIUM CETYL PHOSPHATE, SORBITAN OLIVATE, CARBOMER, MICROCITRUS AUSTRALIS FRUIT EXTRACT, LENS ESCULENTA (LENTIL) FRUIT EXTRACT, PYRUS MALUS (APPLE) FRUIT EXTRACT, CITRULLUS lANATUS (wATERMELON) FRUIT EXTRACT, CITRUS GLAUCA FRUIT EXTRACT, SODIUM LACTATE, PHYTOSPHINGOSINE, ADENOSINE, DECYL GLUCOSIDE, 1,2-HEXANEDIOL, SODIUM PCA, ALPHA-GLUCAN OLIGOSACCHARIDE, MALTODEXTRIN, POLYGLYCERYL-3 CAPRATE, BUTYLENE GLYCOL, AMINOMETHYL PROPANOL, POLYSORBATE 20, CAPRYLHYDROXAMIC ACID, ZINC PCA, THYMOL, TERPINEOL, HEXYLENE GLYCOL, CAPRYLYL GLYCOL, POLYDEXTROSE, DEXTRIN, AMYLOPECTIN, LACTOBACILLUS FERMENT, PHENOXYETHANOL, DISODIUM EDTA, SODIUM BENZOATE, POTASSIUM SORBATE

Other Information

  • STORE IN A COOL, DRY PLACE.

Questions?

VISIT WWW.KATESOMERVILLE.COM OR CALL 1-800-984-5283.

* Please review the disclaimer below.