Home NDC 70677-1056 Foster and Thrive Chest Congestion Relief PE
Product NDC 70677-1056
11-digit product format 706771056
Labeler code 70677
Product ID 70677-1056_92cb8776-6883-4055-9073-17db1a91e71b
Type HUMAN OTC DRUG
Nonproprietary name Guaifenesin/phenylephrine
Dosage form TABLET
Route ORAL
Labeler Strategic Sourcing Services LLC
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-01-27
Substance GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Active strength 400; 10 mg/1; mg/1
Pharmacologic classes Adrenergic alpha1-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], 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 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 70677-1056-1 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 70677-1056-1 f5e01cc5f278…a2eaf40c39c3…
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 Foster and Thrive Chest Congestion Relief PE
Brand name suffix PE
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength GUAIFENESIN 400 mg/1 PHENYLEPHRINE HYDROCHLORIDE 10 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 495W7451VQ Internal UNII lookup 04JA59TNSJ Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1304111 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70677-1056-1 Foster and Thrive Chest Congestion Relief PEPE 50 in 1 BOTTLE TABLET 50 10 70677-1056-1 Foster and Thrive Chest Congestion Relief PEPE 1 in 1 CARTON TABLET 1 10
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70677-1056 FOSTER AND THRIVE CHEST CONGESTION RELIEF PE PE (GUAIFENESIN/PHENYLEPHRINE) TABLET [<TEXT XMLNS="URN:HL7-ORG:V3"> <PARAGRAPH> <CONTENT STYLECODE="BOLD">ACTIVE INGREDIENT</CONTENT> - (PER TABLET)<BR/> <BR/>DEXTROMETHORPHAN HYDROBROMIDE 20MG<BR/> <BR/>GUAIFENESIN 400MG<BR/> </PARAGRAPH> <PARAGRAPH/></TEXT>] 8 Current NDC, 2 package rows 20241225_3429aedc-e83d-498a-bfca-03aaf5847b3b.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 73 of 178 · 3,551 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 70677-1056-1 70677105601 1 BOTTLE in 1 CARTON (70677-1056-1) / 50 TABLET in 1 BOTTLE 1 bottle 2024-12-18 No No Current