Home NDC 41163-503 daytime severe cold
Product NDC 41163-503
11-digit product format 411630503
Labeler code 41163
Product ID 41163-503_0048183a-ab4a-442e-8f89-63e1f0c7f020
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl
Dosage form TABLET, FILM COATED
Route ORAL
Labeler United Natural Foods, Inc. dba UNFI
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2005-08-04
Marketing end 2026-11-30
Substance ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Active strength 325; 10; 200; 5 mg/1; mg/1; mg/1; mg/1
Pharmacologic classes Adrenergic alpha1-Agonists [MoA], 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], alpha-1 Adrenergic Agonist [EPC]
NDC exclude flag No
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 daytime severe cold
Brand name suffix multi-symptom Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 325 mg/1 DEXTROMETHORPHAN HYDROBROMIDE 10 mg/1 GUAIFENESIN 200 mg/1 PHENYLEPHRINE HYDROCHLORIDE 5 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1110988 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 41163-503-08 daytime severe coldmulti-symptom 12 in 1 BLISTER PACK TABLET, FILM COATED 12 18 41163-503-08 daytime severe coldmulti-symptom 2 in 1 CARTON TABLET, FILM COATED 2 18
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ACETAMINOPHEN ACTIVE INGREDIENT 362O9ITL9D DAYTIME SEVERE COLD MULTI-SYMPTOM (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUIAFENESIN, PHENYLEPHRINE HCL) TABLET, FILM COATED [SUPERVALU INC.] 5 DEXTROMETHORPHAN HYDROBROMIDE ACTIVE INGREDIENT 9D2RTI9KYH DAYTIME SEVERE COLD MULTI-SYMPTOM (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUIAFENESIN, PHENYLEPHRINE HCL) TABLET, FILM COATED [SUPERVALU INC.] 5 GUAIFENESIN ACTIVE INGREDIENT 495W7451VQ DAYTIME SEVERE COLD MULTI-SYMPTOM (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUIAFENESIN, PHENYLEPHRINE HCL) TABLET, FILM COATED [SUPERVALU INC.] 5 PHENYLEPHRINE HYDROCHLORIDE ACTIVE INGREDIENT 04JA59TNSJ DAYTIME SEVERE COLD MULTI-SYMPTOM (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUIAFENESIN, PHENYLEPHRINE HCL) TABLET, FILM COATED [SUPERVALU INC.] 5 ACETAMINOPHEN ACTIVE MOIETY 362O9ITL9D DAYTIME SEVERE COLD MULTI-SYMPTOM (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUIAFENESIN, PHENYLEPHRINE HCL) TABLET, FILM COATED [SUPERVALU INC.] 5 DEXTROMETHORPHAN ACTIVE MOIETY 7355X3ROTS DAYTIME SEVERE COLD MULTI-SYMPTOM (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUIAFENESIN, PHENYLEPHRINE HCL) TABLET, FILM COATED [SUPERVALU INC.] 5 GUAIFENESIN ACTIVE MOIETY 495W7451VQ DAYTIME SEVERE COLD MULTI-SYMPTOM (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUIAFENESIN, PHENYLEPHRINE HCL) TABLET, FILM COATED [SUPERVALU INC.] 5 PHENYLEPHRINE ACTIVE MOIETY 1WS297W6MV DAYTIME SEVERE COLD MULTI-SYMPTOM (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUIAFENESIN, PHENYLEPHRINE HCL) TABLET, FILM COATED [SUPERVALU INC.] 5 D&C YELLOW NO. 10 INACTIVE INGREDIENT 35SW5USQ3G DAYTIME SEVERE COLD MULTI-SYMPTOM (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUIAFENESIN, PHENYLEPHRINE HCL) TABLET, FILM COATED [SUPERVALU INC.] 5 MAGNESIUM STEARATE INACTIVE INGREDIENT 70097M6I30 DAYTIME SEVERE COLD MULTI-SYMPTOM (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUIAFENESIN, PHENYLEPHRINE HCL) TABLET, FILM COATED [SUPERVALU INC.] 5 MALTODEXTRIN INACTIVE INGREDIENT 7CVR7L4A2D DAYTIME SEVERE COLD MULTI-SYMPTOM (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUIAFENESIN, PHENYLEPHRINE HCL) TABLET, FILM COATED [SUPERVALU INC.] 5 POLYETHYLENE GLYCOLS INACTIVE INGREDIENT 3WJQ0SDW1A DAYTIME SEVERE COLD MULTI-SYMPTOM (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUIAFENESIN, PHENYLEPHRINE HCL) TABLET, FILM COATED [SUPERVALU INC.] 5 POLYVINYL ALCOHOL INACTIVE INGREDIENT 532B59J990 DAYTIME SEVERE COLD MULTI-SYMPTOM (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUIAFENESIN, PHENYLEPHRINE HCL) TABLET, FILM COATED [SUPERVALU INC.] 5 POVIDONES INACTIVE INGREDIENT FZ989GH94E DAYTIME SEVERE COLD MULTI-SYMPTOM (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUIAFENESIN, PHENYLEPHRINE HCL) TABLET, FILM COATED [SUPERVALU INC.] 5 SODIUM STARCH GLYCOLATE TYPE A POTATO INACTIVE INGREDIENT 5856J3G2A2 DAYTIME SEVERE COLD MULTI-SYMPTOM (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUIAFENESIN, PHENYLEPHRINE HCL) TABLET, FILM COATED [SUPERVALU INC.] 5 STEARIC ACID INACTIVE INGREDIENT 4ELV7Z65AP DAYTIME SEVERE COLD MULTI-SYMPTOM (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUIAFENESIN, PHENYLEPHRINE HCL) TABLET, FILM COATED [SUPERVALU INC.] 5 TALC INACTIVE INGREDIENT 7SEV7J4R1U DAYTIME SEVERE COLD MULTI-SYMPTOM (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUIAFENESIN, PHENYLEPHRINE HCL) TABLET, FILM COATED [SUPERVALU INC.] 5 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP DAYTIME SEVERE COLD MULTI-SYMPTOM (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUIAFENESIN, PHENYLEPHRINE HCL) TABLET, FILM COATED [SUPERVALU INC.] 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 41163-503 DAYTIME SEVERE COLD MULTI-SYMPTOM (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL) TABLET, FILM COATED [UNITED NATURAL FOODS, INC. DBA UNFI] 18 Current NDC, Legacy NDC, 2 package rows 20250426_cc7c5f1c-76b7-4278-8e2a-5fbc85e022dd.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 76 of 180 · 3,583 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join HEB SF Honey Lemon Cough Drops MENTHOL HEB d09ed4bb-7595-5e54-e053-2a95a90aa109 2025-12-13 Warnings Exact identifier application number: M012 HEB Cherry Cough Drops MENTHOL HEB c198e3c7-5ba7-ece6-e053-2995a90adb38 2025-12-13 Warnings Exact identifier application number: M012 HEB Honey Lemon Cough Drops MENTHOL HEB c19a79bc-9872-2e87-e053-2a95a90a9427 2025-12-13 Warnings Exact identifier application number: M012 Cold and Flu Daytime Nighttime ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DIPHENHYDRAMINE HCL, GUAIFENESIN, PHENYLEPHRINE HCL WALMART INC. 26f55169-4b37-4a36-88ee-064d6e962065 2025-12-12 Warnings Exact identifier application number: M012 Allergy Relief DIPHENHYDRAMINE HCL Walgreen Company 39ce76a3-b7a8-43be-9b61-5c1446cd9e90 2025-12-12 Warnings Exact identifier application number: M012 Cold and Flu maximum strength ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL Rite Aid Corporation ac01206f-a717-4c0b-8a03-fab0a4fd154b 2025-12-12 Warnings Exact identifier application number: M012 Sinus Severe ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL Strategic Sourcing Services LLC dcb80dd5-465d-4792-947a-3044e25a5284 2025-12-12 Warnings Exact identifier application number: M012 Vapor Rub COUGH SUPPRESSANT Neilmed Pharmaceuticals Inc. 39190f9f-8a5a-e4d8-e063-6294a90a57dd 2025-12-12 Warnings Exact identifier application number: M012 Medicated Chest Rub CAMPHOR, EUCALYPTUS OIL, MENTHOL Cardinal Health, 110 dba LEADER b7393668-1450-4e85-9793-d400daf39b43 2025-12-12 Warnings Exact identifier application number: M012 Allergy Relief, 24-7 Life by 7-Eleven DIPHENHYDRAMINE HCL TABLET, FILM COATED Lil' Drug Store Products, Inc. 45c4cd6c-327d-5950-e063-6394a90a3a21 2025-12-12 Warnings Exact identifier application number: M012 Menthol cough drops MENTHOL Family Dollar 44bb3b95-b2ba-470e-e054-00144ff88e88 2025-12-12 Warnings Exact identifier application number: M012 menthol cough drops MENTHOL Family Dollar 44bb9c7b-994b-4ab8-e054-00144ff8d46c 2025-12-12 Warnings Exact identifier application number: M012 cherry cough drops MENTHOL Family Dollar 44be9837-f15a-09f2-e054-00144ff8d46c 2025-12-12 Warnings Exact identifier application number: M012 cherry cough drops MENTHOL Family Dollar 44bcae39-2389-09ee-e054-00144ff8d46c 2025-12-12 Warnings Exact identifier application number: M012 honey lemon cough drops MENTHOL Family Dollar 46635813-66c4-504c-e054-00144ff8d46c 2025-12-12 Warnings Exact identifier application number: M012 honey lemon cough drops MENTHOL Family Dollar 455b0f4b-0526-2361-e054-00144ff8d46c 2025-12-12 Warnings Exact identifier application number: M012 Family Wellness Strawberry Cough Drops MENTHOL Family Dollar f92466ac-dd93-9ac5-e053-6294a90a9291 2025-12-12 Warnings Exact identifier application number: M012 GoodSense Menthol Cough Drops MENTHOL Geiss, Destin, Dunn c6b25d69-8930-6867-e053-2a95a90ad208 2025-12-12 Warnings Exact identifier application number: M012 Good Sense Cherry Cough Drops MENTHOL Geiss, Destin, Dunn c72db7f0-9324-8ed2-e053-2995a90a9868 2025-12-12 Warnings Exact identifier application number: M012 Good Sense Honey Lemon Cough Drops MENTHOL Geiss, Destin, Dunn c72e557f-0211-81b9-e053-2995a90a1437 2025-12-12 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 Marketing end Sample Exclude flag Status 41163-503-08 41163050308 2 BLISTER PACK in 1 CARTON (41163-503-08) / 12 TABLET, FILM COATED in 1 BLISTER PACK 2 blister pack 2005-08-04 2026-11-30 No No Current