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Data / Drug companies / Reckitt Benckiser LLC

Reckitt Benckiser LLC: 36 products in the FDA NDC directory, labeler code 59316

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

Reckitt Benckiser LLC (labeler code 59316) lists 36 products in the FDA National Drug Code Directory, covering 5 finished drugs by generic name. By type: 36 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on May 1, 2026.

The request: Watch Reckitt Benckiser LLC (FDA labeler code 59316): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
59316
Products in commercial distribution
36
Packages
90
Finished drugs by generic name
5
Prescription products
0
Over the counter products
36
Flagged as original packager
36 of 36 products that carry the flag
Started marketing in the last 12 months
5
Earliest marketing start
November 1, 2010
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Over the counter monograph drugs36100%

Products by type

TypeProductsShare
Over the counter drugs36100%

Drugs it lists

Finished drugs by generic name, with how many companies list each.

Dosage forms

Dosage formProductsShare
Gel1541.7%
Spray513.9%
Patch513.9%
Kit411.1%
Cream38.3%
Liquid25.6%
Aerosol, spray12.8%
Stick12.8%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Biofreeze Triple Target Gel59316-122GelOver the counter monograph drugsMay 1, 2026
Biofreeze Triple Target Roll-On59316-208GelOver the counter monograph drugsApril 24, 2026
Biofreeze Roll-On and Overnight Roll-On59316-209KitOver the counter monograph drugsApril 1, 2026
Biofreeze Ultraflex Plus59316-898PatchOver the counter monograph drugsJanuary 31, 2026
Biofreeze Professional59316-835SprayOver the counter monograph drugsJanuary 20, 2026
Biofreeze Ultraflex59316-899PatchOver the counter monograph drugsJanuary 15, 2025
BioFreeze Dry Stick59316-230StickOver the counter monograph drugsDecember 28, 2024
Biofreeze59316-870CreamOver the counter monograph drugsFebruary 15, 2024
Biofreeze Professional59316-834Aerosol, sprayOver the counter monograph drugsFebruary 1, 2024
Biofreeze59316-833SprayOver the counter monograph drugsDecember 1, 2023
Biofreeze Day and Overnight59316-832KitOver the counter monograph drugsMay 22, 2023
Biofreeze Overnight Roll-on59316-207GelOver the counter monograph drugsMarch 16, 2023
Biofreeze Overnight Gel59316-121GelOver the counter monograph drugsMarch 1, 2023
Biofreeze Menthol59316-887KitOver the counter monograph drugsMarch 10, 2022
Biofreeze Menthol59316-992PatchOver the counter monograph drugsMarch 4, 2022
Biofreeze Overnight Relief59316-005PatchOver the counter monograph drugsFebruary 1, 2022
Biofreeze Flexible Relief Strip59316-004PatchOver the counter monograph drugsMarch 31, 2021
Biofreeze Foot Pain Relief Set59316-002KitOver the counter monograph drugsMarch 12, 2021
Biofreeze Foot Cream59316-001CreamOver the counter monograph drugsMarch 12, 2021
Biofreeze Precision Relief Pen59316-830LiquidOver the counter monograph drugsDecember 31, 2020
Biofreeze59316-869CreamOver the counter monograph drugsMarch 21, 2020
Biofreeze Foam59316-991LiquidOver the counter monograph drugsJanuary 27, 2020
Biofreeze59316-101GelOver the counter monograph drugsAugust 25, 2016
Biofreeze Professional59316-120SprayOver the counter monograph drugsJune 3, 2016
Biofreeze Professional Colorless Roll-On59316-118GelOver the counter monograph drugsJune 3, 2016

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.