NDC 58118-0608 - Ferrous Sulfate

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
58118-0608
Package NDCs from labels
58118-0608-9, 58118-0608-3, 58118-0608-8, 58118-0608-0
Manufacturer
Clinical Solutions Wholesale
Effective date
2013-08-12
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Ferrous Sulfate - Clinical Solutions WholesaleClinical Solutions Wholesale2013-08-12DIETARY SUPPLEMENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58118-0608-0Ferrous Sulfate1 in 1 PACKAGETABLET13
58118-0608-3Ferrous Sulfate30 in 1 BOTTLE, PLASTICTABLET303
58118-0608-8Ferrous Sulfate30 in 1 BLISTER PACKTABLET303
58118-0608-9Ferrous Sulfate90 in 1 BOTTLE, PLASTICTABLET903

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58118-0608FERROUS SULFATE TABLET [CLINICAL SOLUTIONS WHOLESALE]34 package rows20130812_f886cb50-3791-4c36-ac0d-2c327cd9e3ea.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
FERROUS SULFATEACTIVE INGREDIENT39R4TAN1VTFERROUS SULFATE TABLET [CLINICAL SOLUTIONS WHOLESALE]3
FERROUS CATIONACTIVE MOIETYGW89581OWRFERROUS SULFATE TABLET [CLINICAL SOLUTIONS WHOLESALE]3
CALCIUM CARBONATEINACTIVE INGREDIENTH0G9379FGKFERROUS SULFATE TABLET [CLINICAL SOLUTIONS WHOLESALE]3
CALCIUM STEARATEINACTIVE INGREDIENT776XM7047LFERROUS SULFATE TABLET [CLINICAL SOLUTIONS WHOLESALE]3
CARNAUBA WAXINACTIVE INGREDIENTR12CBM0EIZFERROUS SULFATE TABLET [CLINICAL SOLUTIONS WHOLESALE]3
COCOA BUTTERINACTIVE INGREDIENT512OYT1CRRFERROUS SULFATE TABLET [CLINICAL SOLUTIONS WHOLESALE]3
COPOVIDONE K25-31INACTIVE INGREDIENTD9C330MD8BFERROUS SULFATE TABLET [CLINICAL SOLUTIONS WHOLESALE]3
DIETHYL PHTHALATEINACTIVE INGREDIENTUF064M00AFFERROUS SULFATE TABLET [CLINICAL SOLUTIONS WHOLESALE]3
FD&C RED NO. 40INACTIVE INGREDIENTWZB9127XOAFERROUS SULFATE TABLET [CLINICAL SOLUTIONS WHOLESALE]3
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WOFERROUS SULFATE TABLET [CLINICAL SOLUTIONS WHOLESALE]3
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GFERROUS SULFATE TABLET [CLINICAL SOLUTIONS WHOLESALE]3
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30FERROUS SULFATE TABLET [CLINICAL SOLUTIONS WHOLESALE]3
MALTODEXTRININACTIVE INGREDIENT7CVR7L4A2DFERROUS SULFATE TABLET [CLINICAL SOLUTIONS WHOLESALE]3
METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE AINACTIVE INGREDIENTNX76LV5T8JFERROUS SULFATE TABLET [CLINICAL SOLUTIONS WHOLESALE]3
POLYETHYLENE GLYCOLSINACTIVE INGREDIENT3WJQ0SDW1AFERROUS SULFATE TABLET [CLINICAL SOLUTIONS WHOLESALE]3
POVIDONEINACTIVE INGREDIENTFZ989GH94EFERROUS SULFATE TABLET [CLINICAL SOLUTIONS WHOLESALE]3
POWDERED CELLULOSEINACTIVE INGREDIENTSMD1X3XO9MFERROUS SULFATE TABLET [CLINICAL SOLUTIONS WHOLESALE]3
SHELLACINACTIVE INGREDIENT46N107B71OFERROUS SULFATE TABLET [CLINICAL SOLUTIONS WHOLESALE]3
SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4FERROUS SULFATE TABLET [CLINICAL SOLUTIONS WHOLESALE]3
SODIUM HYDROXIDEINACTIVE INGREDIENT55X04QC32IFERROUS SULFATE TABLET [CLINICAL SOLUTIONS WHOLESALE]3
SODIUM LAURYL SULFATEINACTIVE INGREDIENT368GB5141JFERROUS SULFATE TABLET [CLINICAL SOLUTIONS WHOLESALE]3
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJFERROUS SULFATE TABLET [CLINICAL SOLUTIONS WHOLESALE]3
SUCROSEINACTIVE INGREDIENTC151H8M554FERROUS SULFATE TABLET [CLINICAL SOLUTIONS WHOLESALE]3
TALCINACTIVE INGREDIENT7SEV7J4R1UFERROUS SULFATE TABLET [CLINICAL SOLUTIONS WHOLESALE]3
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPFERROUS SULFATE TABLET [CLINICAL SOLUTIONS WHOLESALE]3
WHITE WAXINACTIVE INGREDIENT7G1J5DA97FFERROUS SULFATE TABLET [CLINICAL SOLUTIONS WHOLESALE]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 173 · 3,454 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
DG health Extra Strength Assorted Fruits AntacidCALCIUM CARBONATEDOLGENCORP, LLC112f1002-c007-4363-ade6-8dfbc61f4b642026-09-03WarningsExact identifier
unii: H0G9379FGK
DG health Extra Strength AntacidSMOOTH DISSOLVE CALCIUM CARBONATEDOLGENCORP, LLCcabaa8f7-9c93-439d-905a-5ef643a08ea82026-09-03WarningsExact identifier
unii: H0G9379FGK
Kids AntacidCALCIUM CARBONATETHE KROGER CO.d77c629b-5308-4b71-9024-9899cf88dbae2026-09-01WarningsExact identifier
unii: H0G9379FGK
Kroger Extra Strength Smooth Antacid Assorted BerryCALCIUM CARBONATEKROGER COMPANY4c8d39d9-9d58-45df-9ffd-2cdc41539c032026-09-01WarningsExact identifier
unii: H0G9379FGK
Kroger Ultra Strength Assorted FruitCALCIUM CARBONATEKROGER COMPANYb60ced06-725c-4dae-abbf-21cab9e431f92026-08-31WarningsExact identifier
unii: H0G9379FGK
Kroger Extra Strength Sugar FreeCALCIUM CARBONATEKROGER COMPANY3f737ce2-961e-4bd0-ae6d-078248cf1c672026-08-31WarningsExact identifier
unii: H0G9379FGK
Kroger Extra Strength Assorted BerryCALCIUM CARBONATEKROGER COMPANYfa191237-d230-4528-8dff-50e8d5c65b6d2026-08-31WarningsExact identifier
unii: H0G9379FGK
BMNP SiliceaSILICEATotal Operations Management LLC DBA:Bestmade Natural Products Micro5a58454f-aed6-24ba-e063-6294a90a47fb2026-08-31WarningsExact identifier
unii: ETJ7Z6XBU4
Kroger Ultra Strength Assorted BerryCALCIUM CARBONATEKROGER COMPANYb7db77a7-0580-455b-a2ef-a68584f039812026-08-31WarningsExact identifier
unii: H0G9379FGK
Ultra Strength Natural AntacidCALCIUM CARBONATEKROGER COMPANY2931d427-b2be-4db9-a58d-ff89c221ff512026-08-31WarningsExact identifier
unii: H0G9379FGK
Ultra Strength AntacidANTACID TABLETSTHE KROGER CO.,f5d82d1b-2f75-4af4-8337-a5bd28c26fb72026-08-31WarningsExact identifier
unii: H0G9379FGK
Kroger Extra Strength Assorted FruitCALCIUM CARBONATEKROGER COMPANY486d7a5f-cbc8-4f86-b12e-c5325bd8c62d2026-08-31WarningsExact identifier
unii: H0G9379FGK
MZANK SUNSCREEN DAILY ULTIMATE PROTECTION SPF50SUNSCREEN SPF50Guangzhou Meixi Biotechnology Co., Ltd.5a0b4bd2-f6ad-35dc-e063-6294a90a8a662026-08-27WarningsExact identifier
unii: 15FIX9V2JP
MELAO Hydrating Lightweight SunscreenAVOBENZONE,ENSULIZOLE,HOMOSALATE,OCTISALATE,OCTOCRYLENE,TITANIUM DIOXIDEGuangdong Aimu Biological Technology Co., Ltd59eeaea1-d726-99f3-e063-6394a90aeea32026-08-26WarningsExact identifier
unii: 15FIX9V2JP
Argentum QuartzARGENTUM QUARTZUriel Pharmacy Inc.765c8c8f-0727-45da-a77e-c3907a3d07932026-08-26WarningsExact identifier
unii: ETJ7Z6XBU4
Endometrium ArgentumENDOMETRIUM ARGENTUMUriel Pharmacy Incd2d1428a-c8b5-9529-e053-2995a90a23432026-08-26WarningsExact identifier
unii: ETJ7Z6XBU4
S12 AIRBORNEALFALFA, ALLIUM SATIVUM, ARSENICUM IODATUM, BARLEY, BETULA PUBESCENS, BROWN RICE, CORN GRAIN, EUPHRASIA OFFICINALIS, FEATHER MIX, HAIR MIX, HISTAMINUM, HOUSE DUST MITE, LOLIUM PERENNE, OAT, PERFOLIATE HONEYSUCKLE, PHLEUM PRATENSE, POLLEN MIX, RYE, SABADILLA, SILICEA, SKIN MIX, SOLIDAGO VIRGAUREA, TARAXACUM OFFICINALE, TEREBINTHINA, WHEATApex Energetics Inc.bb0036c3-1e4d-5750-e053-2995a90ae8952026-08-26WarningsExact identifier
unii: ETJ7Z6XBU4
Pepcid Complete Dual Action Berry FlavorFAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDEJones Healthcare Group - Packaging Services, Incfff07b68-02ca-438e-8d53-5b4edf5eefc52026-08-25WarningsExact identifier
unii: H0G9379FGK
Tumeez Organic AppleCALCIUM CARBONATEBFY LLCf561685a-5260-59c6-e053-2a95a90ae2062026-08-25WarningsExact identifier
unii: H0G9379FGK
Q Skin ScienceSUNSCREENInternational Cosmeceuticals, Inc59e4c3d0-ee4c-2350-e063-6394a90ac9d22026-08-25WarningsExact identifier
unii: 15FIX9V2JP

Reported adverse events (FAERS/openFDA)#

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