---
title: "G-Supress DX (Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl) Pediatric... — FDA record D-0868-2023 | Is It on Recall"
description: "Product mix-up: incorrect product was found inside the G-Supress DX product carton."
url: https://isitonrecall.com/recall/fda-drug-d-0868-2023-g-supress-dx-dextromethorphan-hbr-guaifenesin-phenylephrine-hcl-pediatric-drops-cough-suppressant-ex/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA drug enforcement

# G-Supress DX (Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl) Pediatric Drops Cough Suppressant Expectorant Nas... — FDA record D-0868-2023

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Apr 20, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: 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.) further packaged in a carton, Manufactured in the USA for Kramer Novis, San Juan, PR 00917, NDC 52083-655-01
- **Reason**: Product mix-up: incorrect product was found inside the G-Supress DX product carton.
- **Classification**: Class I
- **Recalling firm**: Novis PR, LLC dba Kramer Novis
- **Quantity**: 9077 bottles
- **Agency-reported status**: Terminated
- **Source record identifier**: D-0868-2023

[Open the official record](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0868-2023%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Lot: D20911, Exp. Oct/25 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Puerto Rico

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Jun 7, 2023
- **Recall initiation date**: Apr 20, 2023
- **Center classification date**: Jun 6, 2023
- **Termination date**: Sep 13, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0868-2023%22)

## Before changing a medicine

Follow urgent instructions in the current official recall notice. Speak to your pharmacist or prescriber before stopping or changing a prescribed medicine.

Talk to your doctor or pharmacist if you have questions or concerns about your medicine. [FDA medication recall guidance](https://www.fda.gov/drugs/drug-recalls/understanding-drug-recalls-what-know-and-what-do)

## Related records

[Medications records](https://isitonrecall.com/category/medications/) [Novis PR, LLC dba Kramer Novis records](https://isitonrecall.com/brand/novis-pr-llc-dba-kramer-novis/)