Home NDC 10956-059 DG Health Immediate Release Mucus Relief
Product NDC 10956-059
11-digit product format 109560059
Labeler code 10956
Product ID 10956-059_1938e502-ee72-400d-933c-271efa88dc69
Type HUMAN OTC DRUG
Nonproprietary name Guaifenesin
Dosage form TABLET
Route ORAL
Labeler Reese Pharmaceutical Co
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2012-08-01
Substance GUAIFENESIN
Active strength 400 mg/1
Pharmacologic classes Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base DG Health Immediate Release Mucus Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength GUAIFENESIN 400 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 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 359601 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 10956-059-30 DG Health Immediate Release Mucus Relief 1 in 1 CARTON TABLET 1 3 10956-059-30 DG Health Immediate Release Mucus Relief 30 in 1 BOTTLE, PLASTIC TABLET 30 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 10956-059 DG HEALTH IMMEDIATE RELEASE MUCUS RELIEF (GUAIFENESIN) TABLET [REESE PHARMACEUTICAL CO] 3 Current NDC, Legacy NDC, 2 package rows 20241220_f60a9d1b-7a63-43d3-b843-e1f31cf78873.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 134 of 196 · 3,909 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Dextromethorphan HBr and Guaifenesin Oral Solution DEXTROMETHORPHAN HBR AND GUAIFENESIN ORAL SOLUTION KESIN PHARMA CORPORATION 284eae44-81bc-400c-e063-6394a90af446 2025-01-30 Warnings Exact identifier application number: M012 Vapor Shower MENTHOL Xiamen Kang Zhongyuan Biotechnology Co., Ltd. 26c82bc3-5753-4d56-96a4-a3f9c8c267d0 2025-01-30 Warnings Exact identifier application number: M012 Vapor Shower MENTHOL Xiamen Kang Zhongyuan Biotechnology Co., Ltd. 8095b211-8ae7-44e5-b89a-b7f730e28d51 2025-01-30 Warnings Exact identifier application number: M012 Vapor Shower MENTHOL Xiamen Kang Zhongyuan Biotechnology Co., Ltd. 2cf2f35b-5d59-e3ff-e063-6294a90a9b45 2025-01-30 Warnings Exact identifier application number: M012 Sinus Congestion and Pain Relief Non-Drowsy, Daytime ACETAMINOPHEN AND PHENYLEPHRINE HCL Rite Aid Corporation 8a0a8abf-0a41-44f8-8f4f-aec68a0fa0c5 2025-01-30 Warnings Exact identifier application number: M012 Mucinex Childrens Mighty Chews Cold and Flu ACETAMINOPHEN AND DEXTROMETHORPHAN HYDROBROMIDE RB Health (US) LLC 2ce20ab5-5f2d-1c97-e063-6394a90ad67b 2025-01-29 Warnings Exact identifier application number: M012 Guaifenesin and Dextromethorphan GUAIFENESIN AND DEXTROMETHORPHAN Major Pharmaceuticals 97b137c9-0bec-409a-91f7-e298c296578b 2025-01-29 Warnings Exact identifier application number: M012 Childrens Mucus and Cough Relief DEXTROMETHORPHAN HBR, GUAIFENESIN CVS 1dc17665-62ce-f7f5-e063-6294a90af851 2025-01-29 Warnings Exact identifier application number: M012 UP AND UP NO DRIP NASAL OXYMETAZOLINE HYDROCHLORIDE Target Corporation 760d6d0f-00fc-40bc-858d-83a0827d139f 2025-01-29 Warnings Exact identifier application number: M012 Guaifenesin and Dextromethorphan GUAIFENESIN AND DEXTROMETHORPHAN Major Pharmaceuticals 51e48201-bb62-4e89-85eb-e4a416f93522 2025-01-29 Warnings Exact identifier application number: M012 Severe Congestion and Cough Max DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL Best Choice 8c878e47-94f4-484f-bdd8-6d87ac2440d8 2025-01-28 Warnings Exact identifier application number: M012 Cough and Cold Therapy CAMPHOR, MENTHOL, EUCALYPTUS OIL Everlaan Organics Inc 088be461-7afc-586a-e063-6294a90a700b 2025-01-27 Warnings Exact identifier application number: M012 Cough and Cold Therapy For Kids CAMPHOR, MENTHOL, EUCALYPTUS OIL Everlaan Organics Inc 088df369-114c-db4f-e063-6394a90acfac 2025-01-27 Warnings Exact identifier application number: M012 Menthol Cough Drops MENTHOL Target Corporation Inc. eb4c2c3f-91d7-e4c6-e053-2a95a90a4e8a 2025-01-26 Warnings Exact identifier application number: M012 Walgreens Menthol Cough Drops MENTHOL Walgreens 2c62f690-8dfb-d28e-e063-6394a90a45a2 2025-01-23 Warnings Exact identifier application number: M012 Walgreens Cherry Cough Drops MENTHOL Walgreens 2c65d836-e724-50d6-e063-6394a90a0827 2025-01-23 Warnings Exact identifier application number: M012 Walgreens Honey Lemon Cough Drops MENTHOL Walgreens 2c67424c-2fb0-cc15-e063-6394a90a02ca 2025-01-23 Warnings Exact identifier application number: M012 Pharmacys Prescription Analgesic Gel MENTHOL American Consumer Products Corp 6f0725f2-833f-f3a0-e053-2a91aa0a3911 2025-01-23 Warnings Exact identifier application number: M012 Pharmacys Prescription Vapor Rub MENTHOL American Consumer Products Corp 6ef328ff-f5c3-515d-e053-2a91aa0a32d3 2025-01-23 Warnings Exact identifier application number: M012 Childrens Allergy Relief DIPHENHYDRAMINE HCL Best Choice 0035e6a4-b3ef-4e0b-aa7f-7453dd065f4d 2025-01-22 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 10956-059-30 10956005930 1 BOTTLE, PLASTIC in 1 CARTON (10956-059-30) / 30 TABLET in 1 BOTTLE, PLASTIC 2013-12-01 0000-00-00 No No Current