Home NDC 69729-143 COLDTAC Plus
Product NDC 69729-143
11-digit product format 697290143
Labeler code 69729
Product ID 69729-143_574a9f60-3b83-0bc7-e063-6294a90a5482
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen, Phenylephrin Hydrochloride, Dextromethorphan Hydrobromide
Dosage form TABLET
Route ORAL
Labeler OPMX LLC
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2018-01-05
Substance ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Active strength 325; 5; 15; 200 mg/1; mg/1; mg/1; mg/1
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 Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 18 matching rows.
View current auxiliary records. · View the auxiliary file history.
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 COLDTAC Plus
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 325 mg/1 PHENYLEPHRINE HYDROCHLORIDE 5 mg/1 DEXTROMETHORPHAN HYDROBROMIDE 15 mg/1 GUAIFENESIN 200 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1367204 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69729-143-02 COLDTAC Plus 2 in 1 POUCH TABLET 2 7 69729-143-06 COLDTAC Plus 6 in 1 PACKAGE TABLET 6 7 69729-143-72 COLDTAC Plus 72 in 1 PACKAGE TABLET 72 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69729-143 COLDTAC PLUS (ACETAMINOPHEN, PHENYLEPHRIN HYDROCHLORIDE, DEXTROMETHORPHAN HYDROBROMIDE) TABLET [OPMX LLC] 7 Current NDC, Legacy NDC, 3 package rows 20240223_3496866c-682f-420b-bfdb-64ecebbf70a2.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 Marketing end Sample Exclude flag Status 69729-143-02 69729014302 2 in 1 POUCH Historical 69729-143-06 69729014306 6 POUCH in 1 PACKAGE (69729-143-06) / 2 TABLET in 1 POUCH 6 pouch 2018-01-05 0000-00-00 No No Current 69729-143-50 69729014350 50 POUCH in 1 CARTON (69729-143-50) / 2 TABLET in 1 POUCH 50 pouch 2026-07-23 No No Current 69729-143-72 69729014372 72 POUCH in 1 PACKAGE (69729-143-72) / 2 TABLET in 1 POUCH 72 pouch 2018-01-05 0000-00-00 No No Current