Home NDC 71800-059 Guaifenesin STRAWBERRY-BANANA FLAVOR
Product NDC 71800-059
11-digit product format 718000059
Labeler code 71800
Product ID 71800-059_37de006a-e717-a4e5-e063-6394a90abd8b
Type HUMAN OTC DRUG
Nonproprietary name GUAIFENESIN
Dosage form LIQUID
Route ORAL
Labeler Innovida Pharmaeutique Corporation
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-06-16
Substance GUAIFENESIN
Active strength 100 mg/5mL
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 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 Guaifenesin STRAWBERRY-BANANA FLAVOR
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength GUAIFENESIN 100 mg/5mL
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 310604 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 71800-059-19 Guaifenesin STRAWBERRY-BANANA FLAVOR 119 mL in 1 TUBE LIQUID 119 1
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 72 of 190 · 3,793 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Daytime Cold and Flu ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE Lil' Drug Store Products, Inc. 5b493ed7-9044-4841-9935-236d0bdc71a9 2025-12-23 Warnings Exact identifier application number: M012 Daytime Cold and Flu ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE Lil' Drug Store Products, Inc. 77a7ff9a-a414-4053-8d8d-369907d4380d 2025-12-23 Warnings Exact identifier application number: M012 Nighttime Cold and Flu ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND DOXYLAMINE SUCCINATE Lil' Drug Store Products, Inc. 8f320235-f243-4211-b99c-18526e686548 2025-12-23 Warnings Exact identifier application number: M012 Circle K Daytime Cold and Flu ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE Lil' Drug Store Products, Inc. b6a46498-d9a8-4da2-9283-57d135f305a5 2025-12-23 Warnings Exact identifier application number: M012 Circle K Nighttime Cold and Flu ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND DOXYLAMINE SUCCINATE Lil' Drug Store Products, Inc. 7c5faec2-28c6-4c15-a268-d8b578140b74 2025-12-23 Warnings Exact identifier application number: M012 Sugar Free Honey Lemon Cough Drops MENTHOL Walmart 67650b94-adbb-87fb-e053-2a91aa0a87e6 2025-12-23 Warnings Exact identifier application number: M012 Equate Benz-Dex Cough and Throat Lozenges BENZOCAINE Walmart c0a6cb7f-a247-e610-e053-2a95a90a4199 2025-12-23 Warnings Exact identifier application number: M012 Equate Honey Lemon Cough Drops MENTHOL WalMart 0028be18-5162-ff51-e063-6294a90ae517 2025-12-23 Warnings Exact identifier application number: M012 Equate SF Menthol Cough Drops MENTHOL WalMart 003a229c-b014-e9f3-e063-6294a90aa5ed 2025-12-23 Warnings Exact identifier application number: M012 Equate Menthol Cough Drops MENTHOL Walmart 124e6968-f59c-39d4-e063-6294a90a66d4 2025-12-23 Warnings Exact identifier application number: M012 Equate Severe Menthol Throat Drop MENTHOL Walmart 125f3f5a-52aa-e398-e063-6394a90a0012 2025-12-23 Warnings Exact identifier application number: M012 Equate Menthol Chewable Gels MENTHOL Walmart 1ba4b2be-7242-0a23-e063-6294a90af29c 2025-12-23 Warnings Exact identifier application number: M012 Walgreens Severe Menthol Throat Drops MENTHOL Walgreens 21dd3c68-cbc6-4799-e063-6394a90a6972 2025-12-23 Warnings Exact identifier application number: M012 cherry throat relief lozenges BENZOCAINE Zee Medical 499d0748-538f-678c-e054-00144ff8d46c 2025-12-23 Warnings Exact identifier application number: M012 Guaiasorb DM DEXTROMETHORPHAN HBR, GUAIFENESIN NuCare Pharmaceuticals, Inc. 46a480c7-7092-b809-e063-6294a90a60cd 2025-12-23 Warnings Exact identifier application number: M012 menthol cough drops MENTHOL Winco Foods 360a6304-206d-5475-e054-00144ff8d46c 2025-12-23 Warnings Exact identifier application number: M012 menthol cough drops MENTHOL Winco Foods 36342d8c-34ab-6178-e054-00144ff8d46c 2025-12-23 Warnings Exact identifier application number: M012 cherry cough drops MENTHOL Winco Foods 37244333-1307-5121-e054-00144ff8d46c 2025-12-23 Warnings Exact identifier application number: M012 honey lemon cough drops MENTHOL Winco foods 37718c73-880e-4a5c-e054-00144ff8d46c 2025-12-23 Warnings Exact identifier application number: M012 honey lemon cough drops MENTHOL Winco Foods 40676ddc-577f-5cc9-e054-00144ff88e88 2025-12-23 Warnings Exact identifier application number: M012
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 71800-059-19 71800005919 119 mL in 1 TUBE (71800-059-19) 119 ml 2025-06-16 No No Current