NDC 0498-7501-01 - Cedaprin

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
0498-7501
Requested NDC
0498-7501-01
Package NDCs from labels
0498-7501-01, 0498-7501-10, 0498-7501-25, 0498-7501-50
Manufacturer
Honeywell Safety Products USA, Inc
Effective date
2024-01-19
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Cedaprin - Honeywell Safety Products USA, IncHoneywell Safety Products USA, Inc2024-01-19HUMAN OTC DRUG LABEL

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
IBUPROFENACTIVE INGREDIENTWK2XYI10QMCEDAPRIN (IBUPROFEN) TABLET [NORTH SAFETY PRODUCTS LLC ]1
IBUPROFENACTIVE MOIETYWK2XYI10QMCEDAPRIN (IBUPROFEN) TABLET [NORTH SAFETY PRODUCTS LLC ]1
CARNAUBA WAXINACTIVE INGREDIENTR12CBM0EIZCEDAPRIN (IBUPROFEN) TABLET [NORTH SAFETY PRODUCTS LLC ]1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UCEDAPRIN (IBUPROFEN) TABLET [NORTH SAFETY PRODUCTS LLC ]1
CROSCARMELLOSE SODIUMINACTIVE INGREDIENTM28OL1HH48CEDAPRIN (IBUPROFEN) TABLET [NORTH SAFETY PRODUCTS LLC ]1
D&C YELLOW NO. 10INACTIVE INGREDIENT35SW5USQ3GCEDAPRIN (IBUPROFEN) TABLET [NORTH SAFETY PRODUCTS LLC ]1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKCEDAPRIN (IBUPROFEN) TABLET [NORTH SAFETY PRODUCTS LLC ]1
FD&C RED NO. 40INACTIVE INGREDIENTWZB9127XOACEDAPRIN (IBUPROFEN) TABLET [NORTH SAFETY PRODUCTS LLC ]1
FD&C YELLOW NO. 6INACTIVE INGREDIENTH77VEI93A8CEDAPRIN (IBUPROFEN) TABLET [NORTH SAFETY PRODUCTS LLC ]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30CEDAPRIN (IBUPROFEN) TABLET [NORTH SAFETY PRODUCTS LLC ]1
MALTODEXTRININACTIVE INGREDIENT7CVR7L4A2DCEDAPRIN (IBUPROFEN) TABLET [NORTH SAFETY PRODUCTS LLC ]1
POLYDEXTROSEINACTIVE INGREDIENTVH2XOU12IECEDAPRIN (IBUPROFEN) TABLET [NORTH SAFETY PRODUCTS LLC ]1
POLYETHYLENE GLYCOLINACTIVE INGREDIENT3WJQ0SDW1ACEDAPRIN (IBUPROFEN) TABLET [NORTH SAFETY PRODUCTS LLC ]1
SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4CEDAPRIN (IBUPROFEN) TABLET [NORTH SAFETY PRODUCTS LLC ]1
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPCEDAPRIN (IBUPROFEN) TABLET [NORTH SAFETY PRODUCTS LLC ]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 16 of 192 · 3,830 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
topcare dual actionACETAMINOPHEN, IBUPROFENTopco Associates LLCdddc04c4-d500-4d42-8406-89f27a9ad6512026-06-04WarningsExact identifier
unii: WK2XYI10QM
ANESSA PERFECT UV SUNSCREEN SKINCARE MILK GBZINC OXIDE OCTOCRYLENE ETHYLHEXYL SALICYLATE HOMOSALATE TITANIUM DIOXIDEHONGKONG JIAHE INTERNATIONAL HOLDING LIMITED5354af18-50c4-5fba-e063-6394a90ace392026-06-03WarningsExact identifier
unii: 15FIX9V2JP
BM Silicea Icing SugarSILICEA ICING SUGARTotal Operations Management LLC DBA:Bestmade Natural Products Micro535ba100-627f-36b4-e063-6394a90a33732026-06-03WarningsExact identifier
unii: ETJ7Z6XBU4
Rohto Digi-EyeHYPROMELLOSE, TETRAHYDROZOLINE HYDROCHLORIDEThe Mentholatum Company5d6f37b9-b568-4cb6-92de-eb40779f3f8c2026-06-03WarningsExact identifier
unii: 3NXW29V3WO
Basic Care IbuprofenIBUPROFENAmazon.com Services LLC4c1a1543-a2a2-43fb-901c-cf6bcc374a3f2026-06-03WarningsExact identifier
unii: WK2XYI10QM
ATOMY BB SUNSCREENTITANIUM DIOXIDE, ZINC OXIDEATOMY CO., LTD.b0cd27ee-4917-4800-bcdf-c6e14b28c1d12026-06-02WarningsExact identifier
unii: 15FIX9V2JP
Atomy Sunscreen White Broad Spectrum SPF 50 PLUSHOMOSALATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDEATOMY CO., LTD.ad0b9091-a990-45bf-93f4-d886be1bbffe2026-06-02WarningsExact identifier
unii: 15FIX9V2JP
Atomy Sunscreen Beige Broad Spectrum SPF 50 PLUSHOMOSALATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDEATOMY CO., LTD.994d5680-284e-4faf-a29b-4d28f8d46e8f2026-06-02WarningsExact identifier
unii: 15FIX9V2JP
Matte Veil Tinted Broad Spectrum Sunscreen SPF 40ZINC OXIDE, TITANIUM DIOXIDEPrivate Label Skin Carea8d60212-18a7-42af-8bb3-bfcff7690a492026-06-02WarningsExact identifier
unii: 15FIX9V2JP
The Mineral Melt SPF30ZINC OXIDE, TITANIUM DIOXIDEDune Suncare Inc.2114fc3b-c8ce-45d2-8a82-4dc54f0adaf32026-06-02WarningsExact identifier
unii: 15FIX9V2JP
LA ROCHE POSAY LABORATOIRE DERMATOLOGIQUE ANTHELIOS UV AIR MINERAL SERUM SUNSCREEN BROAD SPECTRUM SPF 50TITANIUM DIOXIDE AND ZINC OXIDELOreal USA Products Inca1acb789-5bf4-4447-b3c5-4a7d4d3013a72026-06-01WarningsExact identifier
unii: 15FIX9V2JP
BM Tooth RemineralizationCALC PHOS, CALC FLUOR, SILICEABM Private Limited5331dc40-2ac8-5fce-e063-6394a90a58752026-06-01WarningsExact identifier
unii: ETJ7Z6XBU4
Period Pills by BiikayACETAMINOPHEN, IBUPROFENKai Squared40d2ae73-82cf-3fa1-e063-6394a90a9ea22026-06-01WarningsExact identifier
unii: WK2XYI10QM
childrens ibuprofenIBUPROFENCVS Pharmacy6d047655-2b29-4f74-ac6e-93b02c25870c2026-06-01WarningsExact identifier
unii: WK2XYI10QM
IbuprofenIBUPROFENRedpharm Drug5302291e-4816-8495-e063-6394a90a9cc02026-05-30Boxed warning, Warnings, Adverse reactionsExact identifier
unii: WK2XYI10QM
KIEHLS DERMATOLOGIST SOLUTIONS BETTER SCREEN MINER ALL UV SERUM BROAD SPECTRUM SPF 50 PLUS MINERAL SUNSCREENTITANIUM DIOXIDE AND ZINC OXIDELOreal USA Products Inc294e6049-12b5-4b45-ae00-8ee1d9d2a1a42026-05-29WarningsExact identifier
unii: 15FIX9V2JP
IbuprofenIBUPROFENWal-Mart Stores Inccb897d65-7e98-4d02-be64-0704416a0f292026-05-28WarningsExact identifier
unii: WK2XYI10QM
IbuprofenIBUPROFENFamily Dollar (FAMILY WELLNESS)5beb7c11-4ed4-4cd4-9c30-3b0c4016316f2026-05-27WarningsExact identifier
application number: ANDA079129
unii: WK2XYI10QM
Childrens IbuprofenIBUPROFENRite Aid Corporation1da544eb-ed4e-4124-bea3-f827f13222702026-05-27WarningsExact identifier
unii: WK2XYI10QM
IbuprofenIBUPROFENFamily Dollar (FAMILY WELLNESS)da16b1a9-0db2-4f2f-bc85-05ea5ab26e1c2026-05-27WarningsExact identifier
application number: ANDA079129
unii: WK2XYI10QM

Reported adverse events (FAERS/openFDA)#

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