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Data / Drug companies / Diphenhydramine hcl, phenylephrine hcl

Diphenhydramine hcl, 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).

Diphenhydramine hcl, 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 kit; liquid; tablet, film coated, and the newest product started marketing on July 5, 2023.

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Companies listing it
6
Products
7
Generic (ANDA) products
0 (0.0%)
Application numbers
1
Routes
Oral
Brand names
Nighttime Cold and Cough Childrens, Allergy Relief Plus Congestion, Allergy Plus Congestion Relief, Sinus Pe Congestion Daytime Nighttime, Sinus Pe Congestion, Childrens Cold and Cough Nighttime, Sinus Pressure and Congestion Relief
openFDA record search
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Companies that list diphenhydramine hcl, phenylephrine hcl

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Walgreen Company2tablet, film coated; kitOver the counter monograph drugsJanuary 19, 2022
CVS Woonsocket Prescription Center, Incorporated1tablet, film coatedOver the counter monograph drugsAugust 9, 2022
Meijer, Inc.1kitOver the counter monograph drugsJuly 5, 2023
Rite Aid Corporation1kitOver the counter monograph drugsJuly 2, 2019
Safeway1liquidOver the counter monograph drugsDecember 31, 2015
Valu Merchandisers Company1liquidOver the counter monograph drugsJune 10, 2022

Dosage forms

Dosage formProductsShare
Kit342.9%
Liquid228.6%
Tablet, film coated228.6%

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.