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Data / Drug companies / Croda Europe Ltd

Croda Europe Ltd: 49 products in the FDA NDC directory, labeler code 58013

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

Croda Europe Ltd (labeler code 58013) lists 49 products in the FDA National Drug Code Directory. By type: 49 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on September 5, 2023.

The request: Watch Croda Europe Ltd (FDA labeler code 58013): each new product listing and each discontinued product. $10 of work on sign-up, no card.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Labeler code
58013
Products in commercial distribution
49
Packages
81
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Started marketing in the last 12 months
0
Earliest marketing start
January 1, 2010
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients49100%

Products by type

TypeProductsShare
Bulk ingredients49100%

Dosage forms

Dosage formProductsShare
Liquid3775.5%
Powder918.4%
Emulsion36.1%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Titanium dioxide58013-0600LiquidBulk ingredientsSeptember 5, 2023
Titanium dioxide58013-0590LiquidBulk ingredientsNovember 5, 2021
Titanium dioxide58013-0580LiquidBulk ingredientsJune 15, 2021
Titanium dioxide58013-8230LiquidBulk ingredientsMay 24, 2021
Titanium dioxide58013-0570LiquidBulk ingredientsMarch 31, 2021
Titanium dioxide58013-0551LiquidBulk ingredientsMarch 29, 2021
Titanium dioxide58013-0560LiquidBulk ingredientsMarch 17, 2021
Titanium dioxide58013-0660LiquidBulk ingredientsFebruary 3, 2021
Titanium dioxide58013-0530LiquidBulk ingredientsFebruary 3, 2021
Titanium dioxide58013-0439EmulsionBulk ingredientsFebruary 3, 2021
Solaveil mzp8-pw-(mv)58013-0520PowderBulk ingredientsDecember 17, 2020
Solaveil mzp7-pw-(mv)58013-0510PowderBulk ingredientsDecember 17, 2020
Solaveil mz7-100-lq-(mv)58013-0500LiquidBulk ingredientsDecember 17, 2020
Solaveil mz3-300-lq-(mv)58013-0490LiquidBulk ingredientsDecember 17, 2020
Solaveil mz3-100-lq-(mv)58013-0480LiquidBulk ingredientsDecember 17, 2020
Zinc oxide58013-0470PowderBulk ingredientsDecember 15, 2020
Titanium dioxide58013-0460LiquidBulk ingredientsApril 5, 2020
Titanium dioxide58013-0450LiquidBulk ingredientsMarch 18, 2020
Titanium dioxide58013-0440LiquidBulk ingredientsFebruary 13, 2020
Titanium dioxide58013-1051PowderBulk ingredientsFebruary 4, 2020
Titanium dioxide58013-1042PowderBulk ingredientsJanuary 30, 2020
Titanium dioxide58013-1041PowderBulk ingredientsJanuary 30, 2020
Titanium dioxide58013-1030LiquidBulk ingredientsNovember 14, 2019
Zinc oxide58013-0900LiquidBulk ingredientsOctober 5, 2018
Titanium dioxide58013-1021PowderBulk ingredientsJuly 17, 2018

CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.