NDC 11673-930 Up And Up Blemish Controlling Apricot Scrub

Salicylic Acid

NDC Product Code 11673-930

NDC 11673-930-15

Package Description: 170 g in 1 TUBE

NDC Product Information

Up And Up Blemish Controlling Apricot Scrub with NDC 11673-930 is a a human over the counter drug product labeled by Target Corporation. The generic name of Up And Up Blemish Controlling Apricot Scrub is salicylic acid. The product's dosage form is emulsion and is administered via topical form.

Labeler Name: Target Corporation

Dosage Form: Emulsion - A dosage form consisting of a two-phase system comprised of at least two immiscible liquids1, one of which is dispersed as droplets (internal or dispersed phase) within the other liquid (external or continuous phase), generally stabilized with one or more emulsifying agents. (Note: Emulsion is used as a dosage form term unless a more specific term is applicable, e.g. cream, lotion, ointment.)

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.

Up And Up Blemish Controlling Apricot Scrub 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/g

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.

  • SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
  • CORN GRAIN (UNII: C1Z9U7094Z)
  • GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
  • COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • CETYL ALCOHOL (UNII: 936JST6JCN)
  • GLYCERYL STEARATE/PEG-100 STEARATE (UNII: RD25J5V947)
  • ACETYLATED LANOLIN ALCOHOLS (UNII: SNN716810P)
  • METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
  • PPG-2 METHYL ETHER (UNII: RQ1X8FMQ9N)
  • APRICOT (UNII: 269CJD5GZ9)
  • LIMONENE, (+/-)- (UNII: 9MC3I34447)
  • WATER (UNII: 059QF0KO0R)
  • CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED) (UNII: Z135WT9208)
  • JUGLANS REGIA SHELL (UNII: PJ10MT7VKA)
  • CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
  • CETYL ACETATE (UNII: 4Q43814HXS)
  • POLYSORBATE 60 (UNII: CAL22UVI4M)
  • TROLAMINE (UNII: 9O3K93S3TK)
  • PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)
  • LINALOOL, (+/-)- (UNII: D81QY6I88E)

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: Target Corporation
Labeler Code: 11673
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: 09-20-2019 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.

Up And Up Blemish Controlling Apricot Scrub Product Label Images

Up And Up Blemish Controlling Apricot Scrub 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 2.0%

Purpose

Acne Treatment

Indications & Usage

Uses for the treatment of acne.

Warnings

For external use only

Otc - When Using

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 eyes. If contact occurs, flush thoroughly with water.

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.

Dosage & Administration

Directions • cover the entire affected area with a thin layer and rinse thoroughly one to three times daily• if bothersome dryness or peeling occurs, reduce application to once a day or every other day• because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor.

Other

Other information •may stain some fabric •store at room temperature

Inactive Ingredient

Inactive ingredients Water, Juglans Regia (Walnut) Shell Powder, Glyceryl Stearate SE, Propylene Glycol, Sodium Laureth Sulfate, Zea Mays (Corn) Kernel Meal, Cocamidopropyl Betaine, Cetearyl Alcohol, Triethanolamine, Cetyl Alcohol, PEG-100 Stearate, Glyceryl Stearate, Cetyl Acetate, Ceteareth-20, Polysorbate 60, Carbomer, Acetylated Lanolin Alcohol, PPG-2-Methyl Ether, Limonene, Linalool, Methylisothiazolinone, Glycerin, Prunus Armeniaca (Apricot) Fruit Extract, Titanium Dioxide (CI177891).

Otc - Questions

Questions or comments?Call toll free 1-800-910-6874

* Please review the disclaimer below.