Rompe Pecho CF

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Rompe Pecho CF
Generic name: DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL
Manufacturer: Efficient Laboratories Inc
Product type: HUMAN OTC DRUG
SPL set ID: 96c4dee1-6e66-4442-a7e3-56e874414c17
SPL ID: 3e6375e6-6668-3453-e063-6394a90add02
Version: 26
Effective date: 2025-09-09
Source export date: 2026-09-28
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:54:22

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 21 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M012	openfda.application_number
brand name		Rompe Pecho CF	openfda.brand_name
generic name		DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL	openfda.generic_name
manufacturer name		Efficient Laboratories Inc	openfda.manufacturer_name
ndc	package	58593-235-10	openfda.package_ndc
ndc	package	58593-235-08	openfda.package_ndc
ndc	package	58593-235-06	openfda.package_ndc
ndc	package	58593-235-04	openfda.package_ndc
ndc	package	58593-235-29	openfda.package_ndc
ndc	product	58593-235	openfda.product_ndc
ndc11	package	58593023506	derived:openfda.package_ndc
ndc11	package	58593023529	derived:openfda.package_ndc
ndc11	package	58593023508	derived:openfda.package_ndc
ndc11	package	58593023510	derived:openfda.package_ndc
ndc11	package	58593023504	derived:openfda.package_ndc
rxcui		1044949	openfda.rxcui
spl id		3e6375e6-6668-3453-e063-6394a90add02	id
spl set id		96c4dee1-6e66-4442-a7e3-56e874414c17	set_id
unii		9D2RTI9KYH	openfda.unii
unii		04JA59TNSJ	openfda.unii
unii		495W7451VQ	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings Do not exceed recommended dosage. Do not use If you are taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions or Parkinson’s disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI; ask your doctor or pharmacist before taking this product.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.