Home NDC 21130-707 tussin
Product NDC 21130-707
11-digit product format 211300707
Labeler code 21130
Product ID 21130-707_8e25becd-a7f8-4f7f-9572-5ff6eb2a59f9
Type HUMAN OTC DRUG
Nonproprietary name Dextromethorphan HBr, Guaifenesin
Dosage form SOLUTION
Route ORAL
Labeler Safeway
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-10-15
Substance DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Active strength 20; 400 mg/20mL; mg/20mL
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 tussin
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DEXTROMETHORPHAN HYDROBROMIDE 20 mg/20mL GUAIFENESIN 400 mg/20mL
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 1020138 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 21130-707-26 tussin 118 mL in 1 BOTTLE SOLUTION 118 2 21130-707-26 tussin 1 in 1 CARTON SOLUTION 1 2 21130-707-34 tussin 237 mL in 1 BOTTLE SOLUTION 237 2 21130-707-34 tussin 1 in 1 CARTON SOLUTION 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 21130-707 TUSSIN (DEXTROMETHORPHAN HBR, GUAIFENESIN) SOLUTION [SAFEWAY] 2 Current NDC, 4 package rows 20241027_cf04bdf7-fed4-4f06-a193-f2e83fcc531c.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 21130-707-26 21130070726 1 BOTTLE in 1 CARTON (21130-707-26) / 118 mL in 1 BOTTLE 1 bottle 2024-10-15 No No Current 21130-707-34 21130070734 1 BOTTLE in 1 CARTON (21130-707-34) / 237 mL in 1 BOTTLE 1 bottle 2024-10-22 No No Current