Class I · High risk
G-Supress DX
Product mix-up: incorrect product was found inside the G-Supress DX product carton.
National Drug Code
Is NDC 52083-0655-01 recalled?
G-Supress DX · 30 mL in 1 BOTTLE (52083-655-01)
Yes — this exact package was recalled
1 FDA recall names the code 52083-0655-01 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride
- Strength
- DEXTROMETHORPHAN HYDROBROMIDE 5 mg/mL; GUAIFENESIN 50…
- Form
- Syrup · Oral
- Labeler
- Kramer Novis
- Type
- Human OTC Drug
- Product code
- 52083-0655
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 52083-0482 See recall 1
- 52083-0622 See recall 1
- 52083-0630 Pecgen Dmx 1
- 52083-0650 Gencontuss 1
- 52083-0660 Sorbugen 1
- 52083-0699 See recall 1
Free recall alerts
Know the day your medication is recalled
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