14141-225 NDC - MATTE PRO DEFENSE BASE MATE CON MULTIPROTECCION DE LA PIEL FPS 20 MATTE FOUNDATION WITH SKIN MULTIPROTECTION SPF 20 CAPUCCINO 310-C (ZINC OXIDE,OCTINOXATE)

Drug Information

Product NDC: 14141-225

Proprietary Name: MATTE PRO DEFENSE Base mate con multiproteccion de la piel FPS 20 Matte foundation with skin multiprotection SPF 20 CAPUCCINO 310-C

Non Proprietary Name: zinc oxide,octinoxate

Active Ingredient(s):
  • 5 g/100mL OCTINOXATE;
  • 4.2 g/100mL ZINC OXIDE


Administration Route(s): TOPICAL

Dosage Form(s): EMULSION

Labeler Information

Labeler Name: Bel Star S.A. (Colombia)
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date:4/14/2021

Package Information

No. Package Code Package Description Billing Unit
114141-225-0130 mL in 1 JAR (14141-225-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC14141-225The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates 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.
PROPRIETARY NAMEMATTE PRO DEFENSE Base mate con multiproteccion de la piel FPS 20 Matte foundation with skin multiprotection SPF 20 CAPUCCINO 310-CThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEzinc oxide,octinoxateThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEEMULSIONThe translation of the dosage form Code submitted by the firm.
ROUTE NAMETOPICALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE4/14/2021This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH FINALProduct 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.
APPLICATION NUMBERpart352This 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.
LABELER NAMEBel Star S.A. (Colombia)Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEOCTINOXATE; ZINC OXIDEAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH5; 4.2 
ACTIVE INGRED UNITg/100mL; g/100mL 

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This page was last updated on: 2/1/2023