Home NDC 69729-790 Pentrexcilina Adult TOTAL RELIEF Multi-Symptom
Product NDC 69729-790
11-digit product format 697290790
Labeler code 69729
Product ID 69729-790_5c3fa67a-9dc0-95a6-e063-6294a90aecdc
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin USP, Phenylephrine Hydrochloride
Dosage form SYRUP
Route ORAL
Labeler OPMX LLC
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-01-15
Substance PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Active strength 10; 500; 26.66; 400 mg/20mL; mg/20mL; mg/20mL; mg/20mL
Pharmacologic classes Adrenergic alpha1-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA], alpha-1 Adrenergic Agonist [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Pentrexcilina Adult TOTAL RELIEF Multi-Symptom
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PHENYLEPHRINE HYDROCHLORIDE 10 mg/20mL ACETAMINOPHEN 500 mg/20mL DEXTROMETHORPHAN HYDROBROMIDE 26.66 mg/20mL GUAIFENESIN 400 mg/20mL
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69729-790-06 Pentrexcilina Adult TOTAL RELIEF Multi-Symptom 177 mL in 1 BOTTLE SYRUP 177 1 69729-790-06 Pentrexcilina Adult TOTAL RELIEF Multi-Symptom 1 in 1 CARTON SYRUP 1 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69729-790 PENTREXCILINA ADULT TOTAL RELIEF MULTI-SYMPTOM (ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN USP, PHENYLEPHRINE HYDROCHLORIDE) SYRUP [OPMX LLC] 1 Current NDC, 2 package rows 20250119_2bef3b6f-456a-5b76-e063-6394a90aa116.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 74 of 180 · 3,583 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 69729-790-06 69729079006 1 BOTTLE in 1 CARTON (69729-790-06) / 177 mL in 1 BOTTLE 1 bottle 2025-01-15 No No Current