NDC 58593-235 – Rompe Pecho CF

Dextromethorphan Hydrobromide 10 mg/5mL; Guaifenesin 100 mg/5mL; Phenylephrine Hydrochloride 5 mg/5mL · Liquid · Oral

Human Otc Drug 1 recall

Product NDC58593-235

Product details

Brand name
Rompe Pecho CF
Generic name
Dextromethorphan HBr, Guaifenesin, Phenylephrine HCL
Labeler
Efficient Laboratories Inc
Dosage form
Liquid
Route
Oral
Marketing category
OTC MONOGRAPH DRUG · M012
Marketed since
October 1, 2007
Marketing end
March 31, 2027
Pharmacologic class
Expectorant; Sigma-1 Agonist; Uncompetitive N-methyl-D-aspartate Receptor Antagonist; alpha-1 Adrenergic Agonist

Active ingredients

Uses, dosage, side effects and warnings for Rompe Pecho →

Package NDC codes (1)

Package NDCDescriptionSince
58593-235-1010 mL in 1 POUCH (58593-235-10)Jan 1, 2019

Recalls mentioning this NDC

Other Rompe Pecho products