NDC 41250-963 Meijer Oil Free Acne Wash Pink Grapefruit Foaming Scrub

Salicylic Acid

NDC Product Code 41250-963

NDC Code: 41250-963

Proprietary Name: Meijer Oil Free Acne Wash Pink Grapefruit Foaming Scrub 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

  • 41250 - Meijer Distribution, Inc
    • 41250-963 - Meijer

NDC 41250-963-15

Package Description: 198.1 mL in 1 TUBE

NDC Product Information

Meijer Oil Free Acne Wash Pink Grapefruit Foaming Scrub with NDC 41250-963 is a a human over the counter drug product labeled by Meijer Distribution, Inc. The generic name of Meijer Oil Free Acne Wash Pink Grapefruit Foaming Scrub is salicylic acid. The product's dosage form is lotion and is administered via topical form.

Labeler Name: Meijer Distribution, Inc

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.

Meijer Oil Free Acne Wash Pink Grapefruit Foaming 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/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.

  • HELIANTHUS ANNUUS SEED WAX (UNII: 42DG15CHXV)
  • C12-15 ALKYL LACTATE (UNII: GC844VRD7E)
  • POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y)
  • PUMMELO (UNII: ET1TN5W71X)
  • SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
  • SODIUM HYDROXIDE (UNII: 55X04QC32I)
  • D&C VIOLET NO. 2 (UNII: 350KA7O6HK)
  • EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)
  • FD&C RED NO. 40 (UNII: WZB9127XOA)
  • NEOPENTYL GLYCOL DICAPRYLATE/DICAPRATE (UNII: VLW429K27K)
  • SODIUM BENZOTRIAZOLYL BUTYLPHENOL SULFONATE (UNII: 0LA2QC9O3Z)
  • POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
  • ASCORBYL PALMITATE (UNII: QN83US2B0N)
  • D&C RED NO. 30 (UNII: 2S42T2808B)
  • BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • CHONDRUS CRISPUS (UNII: OQS23HUA1X)
  • TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
  • WATER (UNII: 059QF0KO0R)
  • COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
  • POLYSORBATE 20 (UNII: 7T1F30V5YH)
  • BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
  • AGAR (UNII: 89T13OHQ2B)
  • MICA (UNII: V8A1AW0880)
  • POTASSIUM CHLORIDE (UNII: 660YQ98I10)
  • WHITE TEA (UNII: O0M3396E09)

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: Meijer Distribution, Inc
Labeler Code: 41250
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: 07-23-2019 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.

Meijer Oil Free Acne Wash Pink Grapefruit Foaming Scrub Product Label Images

Meijer Oil Free Acne Wash Pink Grapefruit Foaming 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 Ingredients

Salicylic acid 2.0%

Purpose

Acne Treatment

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.

Directions

  • Cover the entire affected area with a thin layer and rinse one to three times daily.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.If bothersome dryness or peeling occurs, reduce application to once a day or every other day.

Other

Other Information • may stain some fabrics

Inactive Ingredients

Water, Sodium C14-16 Olefin Sulfonate, Glycerin, Cocamidopropyl Betaine, Helianthus Annuus (Sunflower) Seed Wax, Acrylates Copolymer, Chondrus Crispus Powder (Carrageenan), C12-15 Alkyl Lactate, Disodium EDTA, Cocamidopropyl PG-Dimonium Chloride Phosphate, Citrus Grandis (Grapefruit) Fruit Extract, Polyquaternium-7, Camellia Sinensis Leaf Extract, Ascorbyl Palmitate, Neopentyl Glycol Dicaprylate/Dicaprate, Anthemis Nobilis Flower Extract, Polysorbate 20, Polyvinyl Alcohol, Potassium Chloride, Propylene Glycol, Sodium Chloride, Benzalkonium Chloride, Butylene Glycol, Sodium Benzotriazolyl Butylphenol Sulfonate, Agar, Sodium Hydroxide, Fragrance, Alcohol, Phenethyl Alcohol, PPG-2 Methyl Ether Mica, Titanium Dioxide, Red 30, Red40, Ext. Violet 2

* Please review the disclaimer below.

Previous Code
41250-962
Next Code
41250-964