NDC 14222-1620 Spotless Acne Clearing Treatment

Benzoyl Peroxide

NDC Product Code 14222-1620

NDC 14222-1620-1

Package Description: 1 BOTTLE, PUMP in 1 CARTON > 50 mL in 1 BOTTLE, PUMP

NDC Product Information

Spotless Acne Clearing Treatment with NDC 14222-1620 is a a human over the counter drug product labeled by Rodan & Fields. The generic name of Spotless Acne Clearing Treatment is benzoyl peroxide. The product's dosage form is lotion and is administered via topical form.

Labeler Name: Rodan & Fields

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.

Spotless Acne Clearing Treatment 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.

  • BENZOYL PEROXIDE .025 g/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)
  • GLYCERETH-18 ETHYLHEXANOATE (UNII: IWS58C6V2Y)
  • GLYCERETH-18 (UNII: SA5E43C17C)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
  • ALLANTOIN (UNII: 344S277G0Z)
  • ASCORBYL PALMITATE (UNII: QN83US2B0N)
  • CAPRYLYL GLYCOL (UNII: 00YIU5438U)
  • CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
  • CETYL HYDROXYETHYLCELLULOSE (350000 MW) (UNII: T7SWE4S2TT)
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • CYCLOMETHICONE 6 (UNII: XHK3U310BA)
  • D&C RED NO. 33 (UNII: 9DBA0SBB0L)
  • D&C VIOLET NO. 2 (UNII: 350KA7O6HK)
  • DECYLENE GLYCOL (UNII: S57M60MI88)
  • DIMETHYL ISOSORBIDE (UNII: SA6A6V432S)
  • DOCUSATE SODIUM (UNII: F05Q2T2JA0)
  • ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
  • GINGER (UNII: C5529G5JPQ)
  • HEXYLENE GLYCOL (UNII: KEH0A3F75J)
  • HYALURONATE SODIUM (UNII: YSE9PPT4TH)
  • HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
  • HYDROXYPHENYL PROPAMIDOBENZOIC ACID (UNII: 25KRT26H77)
  • ISOHEXADECANE (UNII: 918X1OUF1E)
  • LEVOMENOL (UNII: 24WE03BX2T)
  • LOWBUSH BLUEBERRY (UNII: G90PX41VP0)
  • METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: 657L0NC5MT)
  • MICA (UNII: V8A1AW0880)
  • MYRISTYL ALCOHOL (UNII: V42034O9PU)
  • OCTENIDINE HYDROCHLORIDE (UNII: U84956NU4B)
  • PENTYLENE GLYCOL (UNII: 50C1307PZG)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • PHYTOSTERYL/OCTYLDODECYL LAUROYL GLUTAMATE (UNII: 65954KGO9Q)
  • PIDOLIC ACID (UNII: SZB83O1W42)
  • POLYGLYCERYL-2 MONOISOSTEARATE (UNII: 7B8OE71MQC)
  • POLYSORBATE 80 (UNII: 6OZP39ZG8H)
  • PROPANEDIOL (UNII: 5965N8W85T)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • REYNOUTRIA JAPONICA ROOT (UNII: 7TRV45YZF7)
  • SODIUM ACRYLOYLDIMETHYLTAURATE-ACRYLAMIDE COPOLYMER (1:1; 90000-150000 MPA.S) (UNII: 5F4963KLHS)
  • SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)
  • SODIUM HYDROXIDE (UNII: 55X04QC32I)
  • SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
  • STANNIC OXIDE (UNII: KM7N50LOS6)
  • TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
  • TOCOPHEROL (UNII: R0ZB2556P8)
  • XANTHAN GUM (UNII: TTV12P4NEE)

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: Rodan & Fields
Labeler Code: 14222
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: 02-13-2019 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.

Spotless Acne Clearing Treatment 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

Benzoyl Peroxide 2.5%

Purpose

Acne Treatment

Uses

For the treatment of acne. Helps keep skin clear of new acne blemishes, acne pimples, blackheads, and whiteheads.

Warnings

For external use only

Otc - When Using

  • When using this productSkin 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.

  • When using this productAvoid unnecessary sun exposure and use a sunscreen.
  • Avoid contact with the eyes, lips, and mouth.
  • Avoid contact with hair and dyed fabrics, which may be bleached by this product.
  • Skin irritation may occur, characterized by redness, burning, itching, peeling, or possibly swelling. Irritation may be reduced by using the product less frequently or in a lower concentration.

Otc - Stop Use

  • Stop and ask a doctorIf skin irritation becomes severe.

Otc - Do Not Use

  • Do not use if you
  • Have very sensitive skin.
  • Are sensitive to benzoyl peroxide.

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

  • Clean the skin thoroughly before applying this product.
  • Dispense 1-2 pumps and cover the entire affected area with a thin even layer one to three times daily. Do not rinse product off face.
  • 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.
  • If going outside, apply sunscreen after using this product. If irritation or sensitivity develops, stop use of both products and ask a doctor.
  • Wash hands after application to help avoid staining fabrics.

Other Information

Store between 15-30°C (59-86°F). This product may bleach hair or dyed fabrics.

Inactive Ingredients

Water, Glycereth-18 Ethylhexanoate, Glycereth-18, Glycerin, Butylene Glycol, Vaccinium Angustifolium (Blueberry) Fruit Extract, Sodium Hyaluronate, Polygonum Cuspidatum Root Extract, Bisabolol, Allantoin, Zingiber Officinale (Ginger) Root Extract, Octenidine HCL, Fragrance, Phytosteryl/Octyldodecyl Lauroyl Glutamate, Methyl Methacrylate Crosspolymer, Myristyl Alcohol, Acrylamide/Sodium Acryloyldimethyltaurate Copolymer, Cyclopentasiloxane, Butyl Hydroxycyclohexane Carboxylate, Dimethyl lsosorbide, Carbomer, Polyglyceryl-2 lsostearate, Sorbitan Oleate, Diethylhexyl Sodium Sulfosuccinate, Cetyl Hydroxyethylcellulose, Cyclohexasiloxane, Polysorbate 80, Xanthan Gum, Hydroxyphenyl Propamidobenzoic Acid, Ascorbyl PaImitate, Tocopherol, PCA, Sodium Citrate, Citric Acid, Sodium Hydroxide, Propanediol, Pentylene Glycol, lsohexadecane, Caprylyl Glycol, 1,2-Hexanediol, Decylene Glycol, Hydroxyacetophenone, Propylene Glycol, Ethylhexylglycerin, Hexylene Glycol, Phenoxyethanol, Citral, Citronellol, Limonene, Linalool, Titanium Dioxide (Cl 77891), Mica, Tin Oxide, Blue 1 (Cl 42090), Red 33 (Cl 17200), Violet 2 (Cl 60725)

Questions

1-888-995-5656

* Please review the disclaimer below.

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