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Data / Drug companies / Acetaminohpen, dextromethorphan hbr, phenylephrine hcl

Acetaminohpen, dextromethorphan hbr, phenylephrine hcl: 6 companies and 7 products in the FDA NDC directory

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

Acetaminohpen, dextromethorphan hbr, phenylephrine hcl is listed in the FDA National Drug Code Directory by 6 companies, with 7 products in commercial distribution. 0 of the products (0.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are capsule, liquid filled; liquid, and the newest product started marketing on February 13, 2023.

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Companies listing it
6
Products
7
Generic (ANDA) products
0 (0.0%)
Application numbers
1
Routes
Oral
Brand names
Severe Cold and Cough Relief Daytime, Daytime Cold and Flu Non Drowsy, Cold and Flu Relief, Cold and Flu Relief Daytime, Daytime Cold and Flu Relief
openFDA record search
api.fda.gov

Companies that list acetaminohpen, dextromethorphan hbr, phenylephrine hcl

Ranked by number of products. Finished drugs in commercial distribution.

CompanyProductsMain dosage formsMain marketing categoryNewest product started
CVS Pharmacy2capsule, liquid filledOver the counter monograph drugsJuly 31, 2019
CVS Woonsocket Prescription Center, Incorporated1liquidOver the counter monograph drugsFebruary 13, 2023
Cardinal Health 110, LLC. DBA Leader1capsule, liquid filledOver the counter monograph drugsAugust 30, 2019
Dolgencorp, Inc. (dollar General & Rexall)1liquidOver the counter monograph drugsMarch 31, 2017
Major Pharmaceuticals1capsule, liquid filledOver the counter monograph drugsJuly 31, 2019
P & L Development, LLC1liquidOver the counter monograph drugsMarch 26, 2021

Dosage forms

Dosage formProductsShare
Capsule, liquid filled457.1%
Liquid342.9%

Marketing categories

Marketing categoryProductsShare
Over the counter monograph drugs7100%

Pharmacologic classes

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.