# FDA recall D-0868-2023

> **Novis PR, LLC dba Kramer Novis** · Class I · drug recall initiated 2023-04-20.

## 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 for recall

Product mix-up: incorrect product was found inside the G-Supress DX product carton.

## Distribution

Puerto Rico

## Key facts

- **Recall number:** D-0868-2023
- **Recalling firm:** Novis PR, LLC dba Kramer Novis
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2023-04-20
- **Report date:** 2023-06-07
- **Termination date:** 2024-09-13

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** San Juan, PR, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0868-2023

## Citation

> AI Analytics. FDA recall D-0868-2023. Retrieved 2026-07-18 from https://api.ai-analytics.org/recall/D-0868-2023. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
