Home NDC 57896-661 Geri-Tussin
Product NDC 57896-661
11-digit product format 578960661
Labeler code 57896
Product ID 57896-661_36d4f688-1765-6357-e063-6394a90aa8ce
Type HUMAN OTC DRUG
Nonproprietary name Dextromethorphan HBr, Guaifenesin
Dosage form LIQUID
Route ORAL
Labeler Geri-Care Pharmaceuticals, Corp
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-05-01
Substance DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Active strength 10; 100 mg/5mL; mg/5mL
Pharmacologic classes 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]
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 Geri-Tussin
Brand name suffix DM
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DEXTROMETHORPHAN HYDROBROMIDE 10 mg/5mL GUAIFENESIN 100 mg/5mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 9D2RTI9KYH Internal UNII lookup 495W7451VQ Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 996520 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 57896-661-08 Geri-TussinDM 237 mL in 1 BOTTLE LIQUID 237 6 57896-661-16 Geri-TussinDM 473 mL in 1 BOTTLE LIQUID 473 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 57896-661 GERI-TUSSIN DM (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [GERI-CARE PHARMACEUTICALS, CORP] 5 Current NDC, Legacy NDC, 2 package rows 20241225_7e2fb43c-a7f1-4c1d-a700-7c6510999c03.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 97 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 Marketing end Sample Exclude flag Status 57896-661-08 57896066108 237 mL in 1 BOTTLE (57896-661-08) 237 ml 2020-12-01 0000-00-00 No No Current 57896-661-16 57896066116 473 mL in 1 BOTTLE (57896-661-16) 473 ml 2019-05-01 0000-00-00 No No Current