NDC 0363-9986 - Cold and Flu Daytime, Nighttime, Multi-Symptom

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
0363-9986
Manufacturer
Walgreens
Effective date
2026-01-19
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Cold and Flu Daytime, Nighttime, Multi-Symptom - WalgreensWalgreens2026-01-19HUMAN OTC DRUG LABEL

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 144 of 428 · 8,553 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
AcetaminophenACETAMINOPHENGranules USA, Inc.96131c7b-bdff-0642-e053-2a95a90a4f322025-12-22WarningsExact identifier
unii: 362O9ITL9D
Acetaminophen Diphenhydramine HClACETAMINOPHEN DIPHENHYDRAMINE HCLGranules USA, Inc.8c9f68e3-fedc-6457-e053-2995a90a045a2025-12-22WarningsExact identifier
unii: 362O9ITL9D
BASIC CARE DAYTIME NIGHTTIME SEVERE COLD AND FLUACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDEAmazon.com Services LLC82e68c65-9898-4106-a2f8-e39d124c703e2025-12-22WarningsExact identifier
application number: M012
Nighttime Cold and Flu ReliefACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATEHarris Teeter, LLC89fd57d2-fe49-41cb-b02e-9643e526cf472025-12-22WarningsExact identifier
application number: M012
rxcui: 1094549
unii: 9D2RTI9KYH
unii: V9BI9B5YI2
unii: 362O9ITL9D
Menthol Cough DropMENTHOLWalgreens464f6645-ca33-1722-e054-00144ff8d46c2025-12-21WarningsExact identifier
application number: M012
Cherry Cough DropsMENTHOLWalgreen Co.47f38e79-c730-21b9-e054-00144ff88e882025-12-21WarningsExact identifier
application number: M012
Cherry Cough DropMENTHOLWalgreen Co.47522852-005a-2a66-e054-00144ff8d46c2025-12-21WarningsExact identifier
application number: M012
Honey Lemon Cough DropMENTHOLWalgreens Co,47653657-80b5-482f-e054-00144ff88e882025-12-21WarningsExact identifier
application number: M012
Honey Lemon Cough DropMENTHOLWalgreen Co.47f89d33-6e0a-4bb4-e054-00144ff88e882025-12-21WarningsExact identifier
application number: M012
Strawberry Cough DropMENTHOL 2.7 MGWalgreen Co.4766afa8-fdaf-05e5-e054-00144ff8d46c2025-12-21WarningsExact identifier
application number: M012
SF Menthol Cough DropMENTHOLWalgreen Co.477b9fc3-c3c5-647e-e054-00144ff8d46c2025-12-21WarningsExact identifier
application number: M012
SF Honey Lemon Cough DropMENTHOLWalgreen Co.477cedee-6bd3-2a34-e054-00144ff8d46c2025-12-21WarningsExact identifier
application number: M012
Cherry Sore Throat LozengeBENZOCAINEWalgreens Co.47e0f809-0b30-2b23-e054-00144ff8d46c2025-12-21WarningsExact identifier
application number: M012
Sugar Free Honey Lemon Cough DropsMENTHOLWalgreen835e276a-493e-1038-e053-2a91aa0a7ea22025-12-21WarningsExact identifier
application number: M012
Walgreens Mixed Berry Benz-Dex LozengesBENZOCAINEWalgreene108731f-6b77-225a-e053-2a95a90ac25c2025-12-21WarningsExact identifier
application number: M012
unii: 9D2RTI9KYH
Cherry Cough DropsMENTHOLWalmart Stores Inc.318e7acb-0ebb-4518-e054-00144ff88e882025-12-21WarningsExact identifier
application number: M012
cherry cough dropsMENTHOLWalmart Stores Inc.316968e1-7715-4caa-e054-00144ff8d46c2025-12-21WarningsExact identifier
application number: M012
Honey Lemon cough dropsMENTHOLWalmart Stores Inc.317bbd33-6087-3af1-e054-00144ff8d46c2025-12-21WarningsExact identifier
application number: M012
Redness and Dry Eye ReliefGLYCERIN, NAPHAZOLINE HYDROCHLORIDEKC Pharmaceuticals, Inc4682f68d-6bdd-d860-e063-6394a90a2b522025-12-21WarningsExact identifier
unii: PDC6A3C0OX
Good Sense Nasal DecongestantPSEUDOEPHEDRINE HCLL. Perrigo Company455b35b4-3969-411b-8036-887615d71e112025-12-21WarningsExact identifier
application number: M012

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.