Home NDC 69822-211 Akin Cough Formula DM Strawberry Banana
Product NDC 69822-211
11-digit product format 698220211
Labeler code 69822
Product ID 69822-211_0b57d80b-329c-212b-e063-6394a90a4e18
Type HUMAN OTC DRUG
Nonproprietary name DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN
Dosage form LIQUID
Route TOPICAL
Labeler Southern Sales & Service, Inc.
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-02-01
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 Akin Cough Formula DM Strawberry Banana
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 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 69822-211-04 Akin Cough Formula DM Strawberry Banana 118 mL in 1 BOTTLE LIQUID 118 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69822-211 AKIN COUGH FORMULA DM STRAWBERRY BANANA (DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN) LIQUID [SOUTHERN SALES & SERVICE, INC.] 2 Current NDC, 1 package rows 20231201_7a81efd8-775d-455e-860f-f3e3b369a0a7.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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 69822-211-04 69822021104 118 mL in 1 BOTTLE (69822-211-04) 118 ml 2023-02-01 No No Current