Class II · Moderate risk
Rompe Pecho DM
Microbial Contamination of Non-Sterile Products
National Drug Code
Is NDC 58593-0275-06 recalled?
Rompe Pecho DM · 178 mL in 1 BOTTLE (58593-275-06)
Yes — this exact package was recalled
1 FDA recall names the code 58593-0275-06 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 HBr, Guaifenesin
- Strength
- DEXTROMETHORPHAN HYDROBROMIDE 10 mg/5mL; GUAIFENESIN 100…
- Form
- Liquid · Oral
- Labeler
- Efficient Laboratories Inc
- Type
- Human OTC Drug
- Product code
- 58593-0275
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
- 58593-0235 Rompe Pecho CF 1
- 58593-0828 Rompe Pecho Max Multi Symptoms 1
- 58593-0829 Rompe Pecho EX 1
Free recall alerts
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