FDA.reportPublic FDA data

NDC 62011-0060-01 - HealthMart Chest Congestion Relief

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
62011-0060
Requested NDC
62011-0060-01
Package NDCs from labels
62011-0060-1, 62011-0060-01
Manufacturer
Strategic Sourcing Services LLC | Reese Pharmaceutical Co | Pharbest
Effective date
2024-12-18
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Drug FactsStrategic Sourcing Services LLC | Reese Pharmaceutical Co | Pharbest2024-12-18HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62011-0060-1HealthMart Chest Congestion Relief1 in 1 CARTONTABLET14
62011-0060-1HealthMart Chest Congestion Relief50 in 1 BOTTLETABLET504

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62011-0060HEALTHMART CHEST CONGESTION RELIEF (GUAIFENESIN) TABLET [STRATEGIC SOURCING SERVICES LLC]4Current NDC, Legacy NDC, 2 package rows20241220_a5d1a8e8-10ba-4fff-b6f7-18c0fde5155c.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
62011-0060-1EA - Each62011-006040c8027a-5e46-4884-8791-a5276b8321c312014-05-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
GuaifenesinACTIVE INGREDIENT495W7451VQHEALTHMART CHEST CONGESTION RELIEF (GUAIFENESIN) TABLET [MCKESSON]1
GuaifenesinACTIVE MOIETY495W7451VQHEALTHMART CHEST CONGESTION RELIEF (GUAIFENESIN) TABLET [MCKESSON]1
COPOVIDONEINACTIVE INGREDIENTD9C330MD8BHEALTHMART CHEST CONGESTION RELIEF (GUAIFENESIN) TABLET [MCKESSON]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30HEALTHMART CHEST CONGESTION RELIEF (GUAIFENESIN) TABLET [MCKESSON]1
MALTODEXTRININACTIVE INGREDIENT7CVR7L4A2DHEALTHMART CHEST CONGESTION RELIEF (GUAIFENESIN) TABLET [MCKESSON]1
SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4HEALTHMART CHEST CONGESTION RELIEF (GUAIFENESIN) TABLET [MCKESSON]1
STEARIC ACIDINACTIVE INGREDIENT4ELV7Z65APHEALTHMART CHEST CONGESTION RELIEF (GUAIFENESIN) TABLET [MCKESSON]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 91 of 225 · 4,496 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
HEB Honey Lemon Cough DropsMENTHOLHEBc19a79bc-9872-2e87-e053-2a95a90a94272025-12-13WarningsExact identifier
application number: M012
Cold and Flu Daytime NighttimeACETAMINOPHEN, DEXTROMETHORPHAN HBR, DIPHENHYDRAMINE HCL, GUAIFENESIN, PHENYLEPHRINE HCLWALMART INC.26f55169-4b37-4a36-88ee-064d6e9620652025-12-12WarningsExact identifier
application number: M012
Allergy ReliefDIPHENHYDRAMINE HCLWalgreen Company39ce76a3-b7a8-43be-9b61-5c1446cd9e902025-12-12WarningsExact identifier
application number: M012
Cold and Flu maximum strengthACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCLRite Aid Corporationac01206f-a717-4c0b-8a03-fab0a4fd154b2025-12-12WarningsExact identifier
application number: M012
unii: 495W7451VQ
Sinus SevereACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCLStrategic Sourcing Services LLCdcb80dd5-465d-4792-947a-3044e25a52842025-12-12WarningsExact identifier
application number: M012
unii: 495W7451VQ
Vapor RubCOUGH SUPPRESSANTNeilmed Pharmaceuticals Inc.39190f9f-8a5a-e4d8-e063-6294a90a57dd2025-12-12WarningsExact identifier
application number: M012
Allergy Relief, 24-7 Life by 7-ElevenDIPHENHYDRAMINE HCL TABLET, FILM COATEDLil' Drug Store Products, Inc.45c4cd6c-327d-5950-e063-6394a90a3a212025-12-12WarningsExact identifier
application number: M012
Menthol cough dropsMENTHOLFamily Dollar44bb3b95-b2ba-470e-e054-00144ff88e882025-12-12WarningsExact identifier
application number: M012
menthol cough dropsMENTHOLFamily Dollar44bb9c7b-994b-4ab8-e054-00144ff8d46c2025-12-12WarningsExact identifier
application number: M012
cherry cough dropsMENTHOLFamily Dollar44be9837-f15a-09f2-e054-00144ff8d46c2025-12-12WarningsExact identifier
application number: M012
cherry cough dropsMENTHOLFamily Dollar44bcae39-2389-09ee-e054-00144ff8d46c2025-12-12WarningsExact identifier
application number: M012
honey lemon cough dropsMENTHOLFamily Dollar46635813-66c4-504c-e054-00144ff8d46c2025-12-12WarningsExact identifier
application number: M012
honey lemon cough dropsMENTHOLFamily Dollar455b0f4b-0526-2361-e054-00144ff8d46c2025-12-12WarningsExact identifier
application number: M012
Family Wellness Strawberry Cough DropsMENTHOLFamily Dollarf92466ac-dd93-9ac5-e053-6294a90a92912025-12-12WarningsExact identifier
application number: M012
GoodSense Menthol Cough DropsMENTHOLGeiss, Destin, Dunnc6b25d69-8930-6867-e053-2a95a90ad2082025-12-12WarningsExact identifier
application number: M012
Good Sense Cherry Cough DropsMENTHOLGeiss, Destin, Dunnc72db7f0-9324-8ed2-e053-2995a90a98682025-12-12WarningsExact identifier
application number: M012
Good Sense Honey Lemon Cough DropsMENTHOLGeiss, Destin, Dunnc72e557f-0211-81b9-e053-2995a90a14372025-12-12WarningsExact identifier
application number: M012
Good Sense Cherry Benzocaine LozengesBENZOCAINEGeiss, Destin, Dunnc7404c94-09eb-5cc5-e053-2995a90af0212025-12-12WarningsExact identifier
application number: M012
Good Sense SF Honey Lemon Cough DropsMENTHOLGeiss, Destin, Dunne11ed21f-6ceb-5908-e053-2995a90aea462025-12-12WarningsExact identifier
application number: M012
Severe Congestion Relief Maximum Strength SinusACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCLWal-Mart Stores Inc59918b8b-5c91-468f-834e-66020dc1ae122025-12-12WarningsExact identifier
application number: M012
unii: 495W7451VQ

Reported adverse events (FAERS/openFDA)#

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