NDC 47682-060-99 - Medi-First Non-Aspirin

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
47682-060
Requested NDC
47682-060-99
Package NDCs from labels
47682-060-99, 47682-060-13
Manufacturer
Unifirst First Aid Corporation
Effective date
2025-09-08
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Medi-First Non-Aspirin - Unifirst First Aid CorporationUnifirst First Aid Corporation2025-09-08HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47682-060-13Dover Aminofen250 in 1 BOXTABLET, COATED25026
47682-060-99Dover Aminofen2 in 1 PACKETTABLET, COATED226

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
47682-060MEDI-FIRST NON-ASPIRIN (ACETAMINOPHEN) TABLET, COATED MEDIQUE APAP (ACETAMINOPHEN) TABLET, COATED MEDI-FIRST PLUS NON-ASPIRIN (ACETAMINOPHEN) TABLET, COATED MEDI FIRST PLUS NON-ASPIRIN (ACETAMINOPHEN) TABLET, COATED DOVER AMINOPHEN (ACETAMINOPHEN) TABLET, COATED DOVER AMINOFEN (ACETAMINOPHEN) TABLET, COATED [UNIFIRST FIRST AID CORPORATION]25Current NDC, 2 package rows20250210_04805d9c-d959-4870-a185-48b58a880880.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ACETAMINOPHENACTIVE INGREDIENT362O9ITL9DMEDIQUE APAP (ACETAMINOPHEN) TABLET, FILM COATED MEDI-FIRST NON-ASPIRIN (ACETAMINOPHEN) TABLET, FILM COATED MEDI FIRST PLUS NON-ASPIRIN (ACETAMINOPHEN) TABLET, FILM COATED DOVER AMINOPHEN (ACETAMINOPHEN) TABLET, FILM COATED [UNIFIRST FIRST AID CORPORATION]3
ACETAMINOPHENACTIVE MOIETY362O9ITL9DMEDIQUE APAP (ACETAMINOPHEN) TABLET, FILM COATED MEDI-FIRST NON-ASPIRIN (ACETAMINOPHEN) TABLET, FILM COATED MEDI FIRST PLUS NON-ASPIRIN (ACETAMINOPHEN) TABLET, FILM COATED DOVER AMINOPHEN (ACETAMINOPHEN) TABLET, FILM COATED [UNIFIRST FIRST AID CORPORATION]3
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WOMEDIQUE APAP (ACETAMINOPHEN) TABLET, FILM COATED MEDI-FIRST NON-ASPIRIN (ACETAMINOPHEN) TABLET, FILM COATED MEDI FIRST PLUS NON-ASPIRIN (ACETAMINOPHEN) TABLET, FILM COATED DOVER AMINOPHEN (ACETAMINOPHEN) TABLET, FILM COATED [UNIFIRST FIRST AID CORPORATION]3
POLYETHYLENE GLYCOLINACTIVE INGREDIENT3WJQ0SDW1AMEDIQUE APAP (ACETAMINOPHEN) TABLET, FILM COATED MEDI-FIRST NON-ASPIRIN (ACETAMINOPHEN) TABLET, FILM COATED MEDI FIRST PLUS NON-ASPIRIN (ACETAMINOPHEN) TABLET, FILM COATED DOVER AMINOPHEN (ACETAMINOPHEN) TABLET, FILM COATED [UNIFIRST FIRST AID CORPORATION]3
POVIDONEINACTIVE INGREDIENTFZ989GH94EMEDIQUE APAP (ACETAMINOPHEN) TABLET, FILM COATED MEDI-FIRST NON-ASPIRIN (ACETAMINOPHEN) TABLET, FILM COATED MEDI FIRST PLUS NON-ASPIRIN (ACETAMINOPHEN) TABLET, FILM COATED DOVER AMINOPHEN (ACETAMINOPHEN) TABLET, FILM COATED [UNIFIRST FIRST AID CORPORATION]3
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2MEDIQUE APAP (ACETAMINOPHEN) TABLET, FILM COATED MEDI-FIRST NON-ASPIRIN (ACETAMINOPHEN) TABLET, FILM COATED MEDI FIRST PLUS NON-ASPIRIN (ACETAMINOPHEN) TABLET, FILM COATED DOVER AMINOPHEN (ACETAMINOPHEN) TABLET, FILM COATED [UNIFIRST FIRST AID CORPORATION]3
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJMEDIQUE APAP (ACETAMINOPHEN) TABLET, FILM COATED MEDI-FIRST NON-ASPIRIN (ACETAMINOPHEN) TABLET, FILM COATED MEDI FIRST PLUS NON-ASPIRIN (ACETAMINOPHEN) TABLET, FILM COATED DOVER AMINOPHEN (ACETAMINOPHEN) TABLET, FILM COATED [UNIFIRST FIRST AID CORPORATION]3
STEARIC ACIDINACTIVE INGREDIENT4ELV7Z65APMEDIQUE APAP (ACETAMINOPHEN) TABLET, FILM COATED MEDI-FIRST NON-ASPIRIN (ACETAMINOPHEN) TABLET, FILM COATED MEDI FIRST PLUS NON-ASPIRIN (ACETAMINOPHEN) TABLET, FILM COATED DOVER AMINOPHEN (ACETAMINOPHEN) TABLET, FILM COATED [UNIFIRST FIRST AID CORPORATION]3

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 2 of 280 · 5,586 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Cold and Flu HBPACETAMINOPHEN, CHLORPHENIRAMINE MALEATEWALMART INC.f9d1dfd1-527f-491d-9188-14886ac70ced2026-09-08WarningsExact identifier
unii: 362O9ITL9D
Pain Relief Extra StrengthACETAMINOPHENRite Aid Corporationd846065a-5c39-4f4b-894c-4280acaaf4fa2026-09-08WarningsExact identifier
application number: M013
unii: 362O9ITL9D
severe cold and cough daytimeACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDERARITAN PHARMACEUTICALS INC3ce8508e-7d9d-4413-858a-8f952e760c012026-09-08WarningsExact identifier
unii: 362O9ITL9D
Multi Symptom Severe ColdACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCLRARITAN PHARMACEUTICALS INCd9606c9a-31b1-4121-9870-809a05f5b68a2026-09-08WarningsExact identifier
unii: 362O9ITL9D
DESENFRIOL-ITO PLUSACETAMINOPHENOPMX LLC5ac41edd-e845-734d-e063-6294a90a990a2026-09-05WarningsExact identifier
application number: M013
unii: 362O9ITL9D
DRX CHOICE Regular StrengthACETAMINOPHENRaritan Pharmaceuticals Inc.8bacb24a-24d0-4175-b3e0-05efb5f5d3732026-09-05WarningsExact identifier
application number: M013
rxcui: 313782
unii: 362O9ITL9D
Severe Congestion and PainACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCLMeijer Distribution, Inc.49235f4f-e661-4a83-88ef-b9a9568487772026-09-04WarningsExact identifier
unii: 362O9ITL9D
NIGHTTIME COLD AND FLUACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATEAmazon.com Services LLC774d2bde-9f57-4ced-800a-cada39c685ed2026-09-04WarningsExact identifier
unii: 362O9ITL9D
FRESHKOTE PRESERVATIVE FREE LUBRICANT EYE DROPSPOVIDONE, POLYVINYL ALCOHOL SOLUTIONHarrow Eye, LLC049e9cc9-0663-53bc-e063-6294a90a2c4f2026-09-04WarningsExact identifier
unii: FZ989GH94E
Butalbital, Acetaminophen, CaffeineBUTALBITAL, ACETAMINOPHEN, AND CAFFEINEREMEDYREPACK INC.dc2bb7fc-1722-4865-a02c-be5e5c2115052026-09-03Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 362O9ITL9D
Feverall Jr. StrengthACETAMINOPHENSun Pharmaceutical Industries, Inc.3561bbc3-53b0-4857-8b71-39e165ed95ce2026-09-03WarningsExact identifier
unii: 362O9ITL9D
infants pain and feverACETAMINOPHENCVS Pharmacy53b06c48-598e-41ad-ac7a-5508c195535c2026-09-03WarningsExact identifier
application number: M013
unii: 362O9ITL9D
Aspirin Regular StrengthASPIRINCardinal Health 110, LLC. DBA Leader2777beea-06d7-4ff5-ae4a-ad7a117dfb622026-09-02WarningsExact identifier
application number: M013
AMAZON BASIC CARE ACETAMINOPHENACETAMINOPHENAmazon.com Services LLC113d92bf-f6c9-cc3d-e063-6294a90af0332026-09-02WarningsExact identifier
application number: M013
rxcui: 313782
unii: 362O9ITL9D
Childrens Multi Symptom Fever and ColdACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCLTHE KROGER CO.3daf7620-eb57-43d5-ba88-938b7221e3462026-09-02WarningsExact identifier
unii: 362O9ITL9D
Extra Strength Pain RelieverACETAMINOPHENShield Pharmaceuticals Corp.78052120-40d8-4a3f-b72f-cc78ca76213b2026-09-02WarningsExact identifier
application number: M013
unii: 362O9ITL9D
Nighttime Cold and Flu Multi Symptom ReliefACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATEShield Pharmaceuticals Corpdecafa3a-3734-4161-bab0-1219458818462026-09-02WarningsExact identifier
unii: 362O9ITL9D
Nighttime Severe Cold and CoughACETAMINOPHEN, DIPHENHYDRAMINE, PHENYLEPHRINEKROGER COMPANY7def6781-0881-46bf-ad7a-7a3f23a8d9f72026-09-02WarningsExact identifier
unii: 362O9ITL9D
Maximum Strength Cold Flu and Sore ThroatACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCLKROGER COMPANYe1d27123-358f-4b0c-8e3b-33474750a0e62026-09-02WarningsExact identifier
unii: 362O9ITL9D
Kroger Nighttime Cold and Flu ReliefACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATEKroger Companyc5ce0901-a5d7-46c4-8492-5a80c76e85172026-09-02WarningsExact identifier
unii: 362O9ITL9D

Reported adverse events (FAERS/openFDA)#

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