Class III · Low risk
Guaifenesin and Codeine Phosphate Oral Solution USP
Superpotent; sodium benzoate preservative
National Drug Code
Is NDC 0121-0775-16 recalled?
Guaifenesin and Codeine Phosphate · 473 mL in 1 BOTTLE (0121-0775-16)
Yes — this exact package was recalled
1 FDA recall names the code 0121-0775-16 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
- Guaifenesin and Codeine Phosphate
- Strength
- GUAIFENESIN 100 mg/5mL; CODEINE PHOSPHATE 10 mg/5mL
- Form
- Solution · Oral
- Labeler
- PAI Holdings, LLC
- Type
- Human OTC Drug · DEA CV
- Product code
- 0121-0775
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
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