Quick answers
- What is Supress?
- Supress is a brand name of Dextromethorphan, guaifenesin and phenylephrine, Dexbrompheniramine, dextromethorphan and phenylephrine, Guaifenesin and phenylephrine and Dextromethorphan and guaifenesin, an over-the-counter medicine. The FDA NDC Directory lists 8 Supress products in 4 strengths and forms.
- Who makes Supress?
- Kramer Novis lists 7 of the 8 Supress products in the FDA NDC Directory.
- Is there a generic or store brand of Supress?
- Other products of Dextromethorphan, guaifenesin and phenylephrine, Dexbrompheniramine, dextromethorphan and phenylephrine, Guaifenesin and phenylephrine and Dextromethorphan and guaifenesin are listed with the FDA, but none in exactly the same strength and form as a Supress product.
- Has Supress been recalled?
- FDA enforcement reports list 1 recall of Supress products; the newest started April 20, 2023. A recall usually concerns specific lots, not every product.
What Supress is
Each Supress product as listed in the FDA NDC Directory, by active ingredient, strength and form, with its official label. “Same medicine, other names” counts the other products with exactly the same active ingredients, strength and form (generic versions, store brands and other brands); inactive ingredients can differ.
Dextromethorphan, guaifenesin and phenylephrine · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| dextromethorphan hydrobromide 5 mg/mL · guaifenesin 50 mg/mL · phenylephrine hydrochloride 2.5 mg/mL syrup (oral) | Supress DX Pediatric Drops, G-Supress DX, G-Supress Dx Pediatric Drops | None listed | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Dextromethorphan, guaifenesin and phenylephrine →
Dexbrompheniramine, dextromethorphan and phenylephrine · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| dexbrompheniramine maleate 1 mg/mL · dextromethorphan hydrobromide 10 mg/mL · phenylephrine hydrochloride 5 mg/mL syrup (oral) | Supress a | None listed | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Dexbrompheniramine, dextromethorphan and phenylephrine →
Guaifenesin and phenylephrine · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| guaifenesin 50 mg/mL · phenylephrine hydrochloride 2.5 mg/mL solution/ drops (oral) | SUPRESS-PE Pediatric | None listed | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Guaifenesin and phenylephrine →
Dextromethorphan and guaifenesin · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| dextromethorphan hydrobromide 5 mg/mL · guaifenesin 50 mg/mL syrup (oral) | Supress DM | None listed | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Dextromethorphan and guaifenesin →
FDA approval
Supress products are sold under an FDA over-the-counter monograph: rules that set the allowed active ingredients, strengths and label wording, so these products do not need an individual FDA approval.
Companies that list Supress
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Supress products.
- Kramer Novis7 products
- Dextrum Laboratories, Inc1 product
Recalls
From FDA enforcement reports, matched by the product’s NDC code or label. A recall usually covers specific lots: check the lot number on your package and ask your pharmacist. Do not stop a medicine on your own.
-
April 20, 2023 · Class I · Terminated · D-0868-2023
Product mix-up: incorrect product was found inside the G-Supress DX product carton.
G-Supress DX (Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl) Pediatric Drops Cough Suppressant Expectorant Nasal Decongestant, Cherry Flavor Sugar & Alcohol Free, packaged in a bottle Net Content: 30 mL (1 oz.) fu — Novis PR, LLC dba Kramer Novis
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- NADAC (National Average Drug Acquisition Cost) 2026 — Centers for Medicare & Medicaid Services (CMS), data.medicaid.gov, list of November 4, 2026, retrieved November 7, 2026
Which names get a brand page: a name the NDC Directory lists for a medicine, held by one company (the FDA application holder, or the company named on most of its products), that is not just a description, and that is not the only product of its medicine.