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Data / Drug companies / Reckitt Benckiser LLC

Reckitt Benckiser LLC: 75 products in the FDA NDC directory, labeler code 72854

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

Reckitt Benckiser LLC (labeler code 72854) lists 75 products in the FDA National Drug Code Directory, covering 23 finished drugs by generic name. By type: 70 over the counter drugs, 5 drugs for further processing. Its main marketing category is over the counter monograph drugs. The newest product started marketing on July 1, 2026.

The request: Watch Reckitt Benckiser LLC (FDA labeler code 72854): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
72854
Products in commercial distribution
75
Packages
105
Finished drugs by generic name
23
Prescription products
0
Over the counter products
70
Flagged as original packager
56 of 56 products that carry the flag
Started marketing in the last 12 months
12
Earliest marketing start
August 1, 2020
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 drugs6789.3%
Drugs for further processing56.7%
Generic drugs (ANDA)22.7%
New drug applications (NDA)11.3%

Products by type

TypeProductsShare
Over the counter drugs7093.3%
Drugs for further processing56.7%

Drugs it lists

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

DrugProductsCompanies listing it
Acetaminophen, dextromethorphan hydrobromide520
Acetaminophen, guaifenesin46
Dextromethorphan hydrobromide317
Dextromethorphan hydrobromide, guaifenesin349
Dextromethorphan hbr and doxylamine succinate21
Hexylresorcinol23
Oxymetazoline hci21
Acetaminophen, dextromethorphan hbr, triprolidine hcl28
Oxymetazoline hydrochloride, acetaminophen and guaifenesin21
Acetaminophen and guaifenesin21
Acetaminophen, dextromethorphan hbr120
Naproxen sodium, dextromethorphan hydrobromide, guaifenesin11
Dextromethorphan hbr, guaifenesin167
Acetaminophen, dextromethorphan hbr and doxylamine succinate15
Naproxen sodium, pseudoephedrine hydrochloride13
Acetaminophen and dextromethorphan hydrobromide16
Benzocaine and menthol, unspecified form12
Hexylresorcinol and menthol11
Dextromethorphan hydrobromide, triprolidine hydrochloride11
Dextromethorphan hbr, guaifenesin and triprolidine hcl11
Fluticasone propionate171
Dextromethorphan hydrobromide and hexylresorcinol11
Lidocaine1216

Dosage forms

Dosage formProductsShare
Kit2128%
Capsule, liquid filled1520%
Solution810.7%
Tablet, coated810.7%
Lozenge56.7%
Tablet, chewable45.3%
Tablet45.3%
Spray34%
Tablet, extended release22.7%
Spray, metered22.7%
Liquid11.3%
Tablet, film coated11.3%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Mucinex Nasal Congestion and Allergy Relief72854-227Spray, meteredGeneric drugs (ANDA)July 1, 2026
Mucinex DS 12HR COLD, FEVER and SINUS72854-223Tablet, extended releaseGeneric drugs (ANDA)July 1, 2026
Mucinex Fast-Max Kickstart Severe Cold and Flu and Mucinex Fast-Max Recharge Nighttime Cold and Flu72854-188KitOver the counter monograph drugsJuly 1, 2026
Mucinex Fast-Max DM Max and Mucinex Fast-Max Nighttime DM Max Value Pack72854-142KitOver the counter monograph drugsJuly 1, 2026
Mucinex Fastmax Nighttime DM MAX72854-141SolutionOver the counter monograph drugsJuly 1, 2026
Mucinex instasoothe sore throat plus cough sugar free72854-268LozengeOver the counter monograph drugsJune 1, 2026
Mucinex Childrens Multi-Symptom Cold and Flu72854-070SolutionOver the counter monograph drugsJune 1, 2026
Mucinex Childrens Night Time Multi-Symptom Cold and Flu72854-063SolutionOver the counter monograph drugsJune 1, 2026
Mucinex Childrens72854-062KitOver the counter monograph drugsJune 1, 2026
Mucinex 12HR Cold and Fever Multi-Symptom72854-001Tablet, extended releaseNew drug applications (NDA)June 1, 2026
Mucinex Childrens Mini Melts Cold and Flu72854-090GranuleOver the counter monograph drugsApril 5, 2026
Mucinex Fast-Max Recharge Nighttime Cold and Flu72854-167SolutionOver the counter monograph drugsMarch 1, 2026
Mucinex Fast-Max Day Cold and Flu and Mucinex Nightshift Night Severe Cold and Flu Maximum Strength72854-169KitOver the counter monograph drugsJuly 1, 2025
Mucinex Fast-Max Severe Congestion and Cough72854-157Tablet, coatedOver the counter monograph drugsJuly 1, 2025
Mucinex Sinus Max Sinus Pressure Severe Congestion72854-219SprayOver the counter monograph drugsJune 1, 2025
Mucinex Sinus Max Clear and Cool Severe Congestion72854-218SprayOver the counter monograph drugsJune 1, 2025
MUCINEX Rapid Clear Pain, Headache and Mucus Congestion and Nighttime Liquid Gels72854-217KitOver the counter monograph drugsJune 1, 2025
Mucinex Rapid Clear Daytime Pain, Headache, and Cough72854-214Capsule, liquid filledOver the counter monograph drugsJune 1, 2025
MUCINEX Rapid Clear Day Night and Clear and Cool Nasal72854-213KitOver the counter monograph drugsJune 1, 2025
Mucinex Sinus Max Clear and Cool72854-211Capsule, liquid filledOver the counter monograph drugsJune 1, 2025
MUCINEX DAY TIME PAIN, HEADACHE and MUCUS CONGESTION and MUCINEX NIGHT TIME HEADACHE, COUGH and FEVER Maximum Strength72854-210KitOver the counter monograph drugsJune 1, 2025
Mucinex Fast-Max Cold and Flu Maximum Strength72854-171Capsule, liquid filledOver the counter monograph drugsJune 1, 2025
MUCINEX FAST-MAX Liquid Gels Day Night Cold and Flu72854-168KitOver the counter monograph drugsJune 1, 2025
Mucinex Fast-Max Severe Congestion and Cough and Mucinex Nighttime Cold and Flu72854-166KitOver the counter monograph drugsJune 1, 2025
Mucinex Fast-Max DM Max and Mucinex Nighttime Cold and Flu72854-165KitOver the counter monograph drugsJune 1, 2025

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.