Home NDC 67091-265 Tussin DM Cough and Chest
Product NDC 67091-265
11-digit product format 670910265
Labeler code 67091
Product ID 67091-265_88d5ba88-a6f2-4cc2-8623-0d0f10016d1e
Type HUMAN OTC DRUG
Nonproprietary name Dextromethorphan HBr, Guaifenesin
Dosage form LIQUID
Route ORAL
Labeler WinCo Foods, LLC
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2014-12-31
Substance DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Active strength 20; 200 mg/10mL; mg/10mL
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 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 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2024-07-10 04:00 UTC · source 2024-07-09 excluded product product 67091-265 D Discontinued by firm excluded / ndc_excluded.zip 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 67091-265 67091-265-18 D Discontinued by firm excluded / ndc_excluded.zip 557ba5c1ecfa…9c80585c8c6e…
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 DM Cough and Chest
Brand name suffix Non Drowsy
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DEXTROMETHORPHAN HYDROBROMIDE 20 mg/10mL GUAIFENESIN 200 mg/10mL
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 67091-265-18 Tussin DM Cough and ChestNon Drowsy 1 in 1 BOX LIQUID 1 6 67091-265-18 Tussin DM Cough and ChestNon Drowsy 118 mL in 1 BOTTLE, PLASTIC LIQUID 118 6
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded DEXTROMETHORPHAN HYDROBROMIDE ACTIVE INGREDIENT 9D2RTI9KYH TUSSIN DM COUGH AND CHEST NON DROWSY (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [WINCO FOODS, LLC] 2 GUAIFENESIN ACTIVE INGREDIENT 495W7451VQ TUSSIN DM COUGH AND CHEST NON DROWSY (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [WINCO FOODS, LLC] 2 DEXTROMETHORPHAN ACTIVE MOIETY 7355X3ROTS TUSSIN DM COUGH AND CHEST NON DROWSY (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [WINCO FOODS, LLC] 2 GUAIFENESIN ACTIVE MOIETY 495W7451VQ TUSSIN DM COUGH AND CHEST NON DROWSY (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [WINCO FOODS, LLC] 2 ANHYDROUS CITRIC ACID INACTIVE INGREDIENT XF417D3PSL TUSSIN DM COUGH AND CHEST NON DROWSY (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [WINCO FOODS, LLC] 2 DEXTROSE INACTIVE INGREDIENT IY9XDZ35W2 TUSSIN DM COUGH AND CHEST NON DROWSY (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [WINCO FOODS, LLC] 2 FD&C RED NO. 40 INACTIVE INGREDIENT WZB9127XOA TUSSIN DM COUGH AND CHEST NON DROWSY (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [WINCO FOODS, LLC] 2 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX TUSSIN DM COUGH AND CHEST NON DROWSY (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [WINCO FOODS, LLC] 2 HIGH FRUCTOSE CORN SYRUP INACTIVE INGREDIENT XY6UN3QB6S TUSSIN DM COUGH AND CHEST NON DROWSY (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [WINCO FOODS, LLC] 2 MENTHOL, UNSPECIFIED FORM INACTIVE INGREDIENT L7T10EIP3A TUSSIN DM COUGH AND CHEST NON DROWSY (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [WINCO FOODS, LLC] 2 SACCHARIN SODIUM INACTIVE INGREDIENT SB8ZUX40TY TUSSIN DM COUGH AND CHEST NON DROWSY (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [WINCO FOODS, LLC] 2 SODIUM BENZOATE INACTIVE INGREDIENT OJ245FE5EU TUSSIN DM COUGH AND CHEST NON DROWSY (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [WINCO FOODS, LLC] 2 WATER INACTIVE INGREDIENT 059QF0KO0R TUSSIN DM COUGH AND CHEST NON DROWSY (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [WINCO FOODS, LLC] 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 67091-265 TUSSIN DM COUGH AND CHEST NON DROWSY (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [WINCO FOODS, LLC] 6 Current NDC, Legacy NDC, 2 package rows 20240926_13eb459c-3075-4038-8062-9ee7175b2ab9.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 130 of 178 · 3,551 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join CVS Vapor Steam CAMPHOR (SYNTHETIC) CVS 49da2c40-afc5-5770-e054-00144ff88e88 2024-12-13 Warnings Exact identifier application number: M012 Kroger Daytime Cold and Flu Softgel ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE The Kroger Company e428dd83-c538-2a92-e053-2a95a90a0e16 2024-12-13 Warnings Exact identifier application number: M012 Kroger Nighttime Cold and Flu Softgel ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE The Kroger Company e46291c7-6f4d-46a2-e053-2a95a90a80a1 2024-12-13 Warnings Exact identifier application number: M012 Foster and Thrive Childrens Allergy Relief DIPHENHYDRAMINE HCL Strategic Sourcing Services LLC 7eaba464-5cdb-4bd4-b272-38fa108658d5 2024-12-13 Warnings Exact identifier application number: M012 SUDAFED OM Sinus Severe Original OXYMETAZOLINE HYDROCHLORIDE Kenvue Brands LLC 1d089074-3969-ce6e-e063-6294a90aa70c 2024-12-12 Warnings Exact identifier application number: M012 RIGHT REMEDIES Allergy Relief DIPHENHYDRAMINE HYDROCHLORIDE Strive Pharmaceuticals Inc b4fc014c-7c5f-46a4-bf13-57103b6fa018 2024-12-11 Warnings Exact identifier application number: M012 Diphenhydramine Hydrochloride 25mg DIPHENHYDRAMINE HYDROCHLORIDE 25MG Strive Pharmaceuticals Inc b440eb2e-4de9-2b65-e053-2995a90abda8 2024-12-11 Warnings Exact identifier application number: M012 Meijer Effervescent Cold Relief ASPIRIN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE BITARTRATE Meijer Distribution Inc. 6933ca9d-a32d-d856-e053-2a91aa0a408e 2024-12-10 Warnings Exact identifier application number: M012 Effervescent Orange Cold Relief ASPIRIN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE BITARTRATE Meijer Distribution Inc. 826b5c0d-7a75-bbf0-e053-2a91aa0aebd6 2024-12-10 Warnings Exact identifier application number: M012 DUAL ACTION CHERRY COUGH SUPPRESSANT ORAL ANESTHETIC MENTHOL Ricola USA Inc. 09141018-37ba-4c93-9051-1ed129c448c1 2024-12-10 Warnings Exact identifier application number: M012 Original Herb Cough Drops MENTHOL Ricola USA Inc. 6ac9d95b-f6b9-4515-b126-697f8f839612 2024-12-10 Warnings Exact identifier application number: M012 THE ORIGINAL NATURAL HERB COUGH DROPS MENTHOL Ricola USA Inc. 989d1529-2875-47bf-81df-65494d62be7a 2024-12-10 Warnings Exact identifier application number: M012 DUAL ACTION CHERRY COUGH SUPPRESSANT ORAL ANESTHETIC MENTHOL Ricola USA Inc. 82813342-2be2-4731-ae90-dbd5eed667a9 2024-12-10 Warnings Exact identifier application number: M012 MOUNTAIN HERB SUGAR FREE WITH STEVIA COUGH SUPPRESSANT ORAL ANESTHETIC MENTHOL Ricola USA Inc. b640a5d2-a7fe-486d-a65f-e7c993f950d6 2024-12-10 Warnings Exact identifier application number: M012 Sugar Free Mountain Herb Cough Suppressant Throat Drops MENTHOL Ricola USA Inc. c3f3c062-55e5-43c1-a016-ee47a7b388a5 2024-12-10 Warnings Exact identifier application number: M012 RICOLA MAX THROAT CARE SWISS CHERRY MENTHOL Ricola USA Inc. ee4733b5-6e5a-438a-97da-110f3ef6c809 2024-12-10 Warnings Exact identifier application number: M012 SUGAR FREE GREEN TEA WITH ECHINACEA COUGH SUPPRESSANT THROAT DROPS MENTHOL Ricola USA Inc. f62fcc38-2d43-40b3-841f-c8eea9ebd1e1 2024-12-10 Warnings Exact identifier application number: M012 DUAL ACTION HONEY LEMON COUGH SUPPRESSANT ORAL ANESTHETIC MENTHOL Ricola USA Inc. 8a6db093-7e52-443f-8dd6-94867606fef8 2024-12-10 Warnings Exact identifier application number: M012 RICOLA MAX THROAT CARE COOL PEPPERMINT MENTHOL Ricola USA Inc. 5885343e-4a6e-44f7-87a4-d52599156197 2024-12-10 Warnings Exact identifier application number: M012 EXTRA STRENGTH WITH NATURAL MENTHOL GLACIER MINT COUGH SUPPRESSANT MENTHOL Ricola USA Inc. 0baf383c-886d-47ca-8a6d-221298c79446 2024-12-10 Warnings Exact identifier application number: M012
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 67091-265-18 67091026518 1 BOTTLE, PLASTIC in 1 BOX (67091-265-18) / 118 mL in 1 BOTTLE, PLASTIC 2014-12-31 0000-00-00 No No Current