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Data / Drug companies / Symrise AG

Symrise AG: 13 products in the FDA NDC directory, labeler code 48251

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

Symrise AG (labeler code 48251) lists 13 products in the FDA National Drug Code Directory. By type: 13 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on March 24, 2023.

The request: Watch Symrise AG (FDA labeler code 48251): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
48251
Products in commercial distribution
13
Packages
22
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Controlled substance products
Schedule V 1
Started marketing in the last 12 months
0
Earliest marketing start
September 4, 2002
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients13100%

Products by type

TypeProductsShare
Bulk ingredients13100%

Dosage forms

Dosage formProductsShare
Concentrate969.2%
Powder215.4%
Pellet17.7%
Crystal17.7%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Ensulizole48251-1299PowderBulk ingredientsMarch 24, 2023
Zinc oxide48251-4286PowderBulk ingredientsFebruary 14, 2023
Zinc oxide48251-2590ConcentrateBulk ingredientsFebruary 14, 2023
Zinc oxide48251-2569ConcentrateBulk ingredientsFebruary 14, 2023
Octisalate48251-0314ConcentrateBulk ingredientsMarch 12, 2020
Cannabidiol48251-0300ConcentrateBulk ingredientsApril 4, 2019
Titanium dioxide48251-7046ConcentrateBulk ingredientsJanuary 1, 2015
Methyl salicylate48251-0220ConcentrateBulk ingredientsDecember 10, 2012
Thymol48251-0213CrystalBulk ingredientsSeptember 5, 2002
Octocrylene48251-0113ConcentrateBulk ingredientsSeptember 5, 2002
Racementhol48251-0219ConcentrateBulk ingredientsSeptember 4, 2002
Levomenthol48251-0218PelletBulk ingredientsSeptember 4, 2002
Benzyl benzoate48251-0215ConcentrateBulk ingredientsSeptember 4, 2002

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.