NDC 50544-001 Oil-free Acne Cleanser

NDC Product Code 50544-001

NDC CODE: 50544-001

Proprietary Name: Oil-free Acne Cleanser 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.

NDC Code Structure

  • 50544 - University Medical Pharmaceuticals Corp

NDC 50544-001-06

Package Description: 237 g in 1 BOTTLE, PLASTIC

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Oil-free Acne Cleanser with NDC 50544-001 is a product labeled by University Medical Pharmaceuticals Corp. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 308688.

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)
  • DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
  • GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
  • PEG-100 STEARATE (UNII: YD01N1999R)
  • STEARIC ACID (UNII: 4ELV7Z65AP)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
  • MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
  • LEVOMENOL (UNII: 24WE03BX2T)
  • BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
  • PSEUDOPTEROGORGIA ELISABETHAE (UNII: UDY3H1OUX5)
  • HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
  • MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
  • MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
  • XANTHAN GUM (UNII: TTV12P4NEE)
  • CETYL ALCOHOL (UNII: 936JST6JCN)
  • CETYL ESTERS WAX (UNII: D072FFP9GU)
  • SODIUM BENZOATE (UNII: OJ245FE5EU)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
  • METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: University Medical Pharmaceuticals Corp
Labeler Code: 50544
Start Marketing Date: 11-01-2011 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: 12-31-2017 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: I - INACTIVATED, the listing data was inactivated by the FDA. 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.

Information for Patients

Benzoyl Peroxide Topical

Benzoyl Peroxide Topical is pronounced as (ben' zoe il)

Why is benzoyl peroxide topical medication prescribed?
Benzoyl peroxide is used to treat mild to moderate acne....
[Read More]

* Please review the disclaimer below.

Oil-free Acne Cleanser Product Label Images

Oil-free Acne Cleanser 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

Otc - Active Ingredient

Active Ingredient: Benzoyl Peroxide 2.5% w/v

Otc - Purpose

Purpose: Acne Treatment

Indications & Usage

Use for the treatment of acne.

Warnings

Warnings For external use only.

Otc - Do Not Use

Do not use: If you are sensitive to Benzoyl Peroxide or have very sensitive skin. This product may cause irritation.

Otc - Ask Doctor/Pharmacist

Ask a doctor or pharmacist before use: If you are using other topical acne drugs at the same time or right before use of this product. This may increase dryness, redness or irritation of the skin. If this occurs, only one medication should be used unless a doctor directs otherwise.

Otc - When Using

  • When using this product: Avoid contact with eyes. If contact occurs, flush thoroughly with water. Keep away from lips and mouth. Avoid unnecessary sun exposure and use a sunscreen. Avoid product with hair and dyed fabrics, including carpets and clothing which may be bleached by this product.

Otc - Stop Use

Stop use and ask a doctor: If excessive irritation occurs.

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: Use every morning and evening. Apply a dime-size amount to damp skin and gently massage, avoiding the eye area. Rinse well. If bothersome peeling occurs, reduce application use. May also be used on chest or back.

Inactive Ingredient

Inactive ingredients: Water, Disodium Laureth Sulfosuccinate, Glyceryl Stearate, PEG-100 Stearate, Stearic Acid, Glycerin, Cocamidopropyl Betaine, Bakuchiol, Panthenyl Triacetate, Bisabolol, Benzalkonium Chloride, Chamomilla Recuita (Matricaria) Flower Extract, Naringenin, Sea Whip Extract, Polyethylene, Xanthan Gum, Cetyl Alcohol, Magnesium Aluminum Silicate, Sodium Benzoate, Caprylic/Capric Triglyeride, Farnesol, Phenoxyethanol, Ethylhexylglycerin, Methylisothiazolinone.

* Please review the disclaimer below.