Home NDC 49035-781 NDC 49035-781 - EQUATE Tussin DM Max Daytime Nighttime This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 49035-781
Package NDCs from labels 49035-781-26
Manufacturer Wal-Mart Stores Inc
Effective date 2019-02-07
Current FDA listing Not matched in FDA.report NDC product tables
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 204 of 324 · 6,469 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Pain Relief Patch PAIN RELIEF PATCH Henan Enokon Medical Instrument Co., Ltd. 1592d29d-e275-a44d-e063-6294a90ab17d 2025-04-02 Warnings Exact identifier unii: L7T10EIP3A Eye Wash WATER CMC Group Inc. 6158a1f5-a6bc-4a3e-9d1d-0a310d9dc561 2025-04-02 Warnings Exact identifier unii: 059QF0KO0R up and up nighttime sleep aid DOXYLAMINE SUCCINATE Target Corporation 24a0144d-cbfc-4d2f-873d-86adfa0468ca 2025-04-02 Warnings Exact identifier unii: V9BI9B5YI2 dextromethorphan polistirex extended release DEXTROMETHORPHAN POLISTIREX Bryant Ranch Prepack bd415342-90e1-411b-b6c9-652e9532c611 2025-04-02 Warnings Exact identifier unii: 9D2RTI9KYH Guaifenesin GUAIFENESIN KESIN PHARMA CORPORATION 31b8ad0a-3637-03db-e063-6394a90acdc3 2025-04-01 Warnings Exact identifier application number: M012 unii: 495W7451VQ MUCUS RELIEF GUAIFENESIN Bi-Mart d995a6a5-d68b-44e4-9281-32c5417fb5e3 2025-04-01 Warnings Exact identifier unii: 495W7451VQ CareOne Nighttime Sleep Aid DOXYLAMINE SUCCINATE American Sales Company f8bfc874-53be-41e8-b59c-d538825761a8 2025-04-01 Warnings Exact identifier unii: V9BI9B5YI2 CVS Pain Relief MENTHOL 10.5% CVS d0ea80ce-38b2-acde-e053-2995a90a47e5 2025-03-31 Warnings Exact identifier unii: L7T10EIP3A Pharmacys Prescription Vapor Rub MENTHOL American Consumer Products Corp 31aa54d8-df8d-f1ae-e063-6294a90a9622 2025-03-31 Warnings Exact identifier application number: M012 unii: L7T10EIP3A berkley and jensen sleep aid DOXYLAMINE SUCCINATE BJWC 25f468a9-71d4-40f2-97bb-1c3ff5d4b728 2025-03-31 Warnings Exact identifier unii: V9BI9B5YI2 Guaifenesin GUAIFENESIN Bryant Ranch Prepack 570a71eb-2d19-4c7b-8c00-e1524bfa3844 2025-03-31 Warnings Exact identifier application number: M012 unii: 495W7451VQ SODIUM PHENYLACETATE and SODIUM BENZOATE SODIUM PHENYLACETATE AND SODIUM BENZOATE Ailex Pharmaceuticals, LLC 329655ae-c3c0-46b2-a925-e49777f2076b 2025-03-30 Warnings, Adverse reactions Exact identifier unii: OJ245FE5EU Guaifenesin GUAIFENESIN KESIN PHARMA CORPORATION 365c01b7-a197-4876-85fc-42204f787e3a 2025-03-28 Warnings Exact identifier application number: M012 unii: 495W7451VQ Diphenhydramine HCL DIPHENHYDRAMINE HCL Bryant Ranch Prepack 59aeb692-2f79-45aa-8e6a-dab77cd3b2f9 2025-03-28 Warnings Exact identifier application number: M012 Diphenhydramine Hydrochloride DIPHENHYDRAMINE HYDROCHLORIDE Oncor Pharmaceuticals 06ecba97-c790-4672-a8c3-f9caf6272d26 2025-03-27 Warnings Exact identifier application number: M012 Lidothol LIDOCAINE HCL, MENTHOL Clinic Pharma 3159db23-6439-7c2e-e063-6294a90a310b 2025-03-27 Warnings, Adverse reactions Exact identifier unii: L7T10EIP3A Sugar Free Honey-Lemon Fishermans Friend Menthol Cough Suppressant MENTHOL Lofthouse of Fleetwood, Ltd. 87ebb4d9-78d7-1c87-e053-2a95a90adb7d 2025-03-27 Warnings Exact identifier application number: M012 unii: L7T10EIP3A REVASOL CHILDRENS ALLERGY DIPHENHYDRAMINE HCL Rnv LLC 3143137f-ef42-5358-e063-6394a90a8ed1 2025-03-26 Warnings Exact identifier application number: M012 Parche Leon CAPSAICIN, CAMPHOR, MENTHOL Pharmadel LLC a8f266fa-6e43-559e-e053-2995a90a2c75 2025-03-26 Warnings Exact identifier unii: L7T10EIP3A topcare sleep aid DOXYLAMINE SUCCINATE Topco Associates LLC c8b24ed8-34a1-4857-8fcb-6e3f9d407903 2025-03-26 Warnings Exact identifier unii: V9BI9B5YI2
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.