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United States · US · US:58593-829_26e4f72a-b911-8dc6-e063-6394a90a4326
Rompe Pecho
UNIISPLATC R05CA03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerEfficient Laboratories Inc
CountryUS (United States)
ATC codeR05CA03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc115859382904118 mL in 1 BOTTLE (58593-829-04)
- ndc115859382906178 mL in 1 BOTTLE (58593-829-06)
Annotations
UNII (FDA Substance ID)
495W7451VQ
GUAIFENESIN
RxCUI 5032
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "495W7451VQ",
"rxcui": "5032",
"inchikey": "HSRJKNPTNIJEKV-UHFFFAOYSA-N",
"display_name": "GUAIFENESIN",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"4f86985c-48f3-2148-e063-6394a90ae2f1": {
"match": "brand_token",
"title": "ROMPE PECHO MAX (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [EFFICIENT LABORATORIES INC]",
"spl_version": "1",
"published_date": "2026-04-17"
}
},
"productid": "58593-829_26e4f72a-b911-8dc6-e063-6394a90a4326",
"productndc": "58593-829",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "GUAIFENESIN",
"proprietary_name": "Rompe Pecho",
"active_ingred_unit": "mg/10mL",
"application_number": "M012",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Guaifenesin",
"start_marketing_date": "20150101",
"active_numerator_strength": "200"
}Related drugs
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