Home NDC 58809-218 TexaClear Pain and Chest Congestion Relief
Product NDC 58809-218
11-digit product format 588090218
Labeler code 58809
Product ID 58809-218_41115f01-9ab2-9f2a-e063-6294a90a377c
Type HUMAN OTC DRUG
Nonproprietary name Choline Salicylate,Guaifenesin
Dosage form LIQUID
Route ORAL
Labeler GM Pharmaceuticals, INC
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-10-25
Substance GUAIFENESIN; CHOLINE SALICYLATE
Active strength 200; 870 mg/30mL; mg/30mL
Pharmacologic classes Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
NDC exclude flag No
Listing certified through 2026-12-31
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 TexaClear Pain and Chest Congestion Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength GUAIFENESIN 200 mg/30mL CHOLINE SALICYLATE 870 mg/30mL
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 KD510K1IQW Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2670549 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 58809-218-08 TexaClear Pain and Chest Congestion Relief 237 mL in 1 BOTTLE, PLASTIC LIQUID 237 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 58809-218 TEXACLEAR PAIN AND CHEST CONGESTION RELIEF (CHOLINE SALICYLATE,GUAIFENESIN) LIQUID [GM PHARMACEUTICALS, INC] 2 Current NDC, 1 package rows 20241009_672bc78a-2c71-4135-b64a-2b8c40ac688c.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 99 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 58809-218-08 58809021808 237 mL in 1 BOTTLE, PLASTIC (58809-218-08) 237 ml 2023-10-25 No No Current