FDA.reportPublic FDA data

NDC 70518-2190-01 - Amoxicillin

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
70518-2190
Requested NDC
70518-2190-01
Package NDCs from labels
70518-2190-0, 70518-2190-1, 70518-2190-2, 70518-2190-3, 70518-2190-4, 70518-2190-5, 70518-2190-6, 70518-2190-7, 70518-2190-8, 70518-2190-9, 70518-2190-01
Manufacturer
Sportpharm LLC
Effective date
2026-09-29
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Amoxicillin - Sportpharm LLCSportpharm LLC2026-09-29HUMAN PRESCRIPTION DRUG LABEL
Amoxicillin - REMEDYREPACK INC.REMEDYREPACK INC.2026-07-21HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70518-2190-0Amoxicillin28 in 1 BLISTER PACKCAPSULE2820
70518-2190-1Amoxicillin21 in 1 BLISTER PACKCAPSULE2120
70518-2190-2Amoxicillin30 in 1 BLISTER PACKCAPSULE3020
70518-2190-3Amoxicillin30 in 1 BOTTLE, PLASTICCAPSULE3020
70518-2190-4Amoxicillin21 in 1 BOTTLE, PLASTICCAPSULE2120
70518-2190-5Amoxicillin20 in 1 BOTTLE, PLASTICCAPSULE2020
70518-2190-6Amoxicillin1 in 1 POUCHCAPSULE120
70518-2190-7Amoxicillin100 in 1 BOXCAPSULE10020
70518-2190-8Amoxicillin14 in 1 BOTTLE, PLASTICCAPSULE1420
70518-2190-9Amoxicillin40 in 1 BOTTLE, PLASTICCAPSULE4020

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70518-2190AMOXICILLIN CAPSULE [REMEDYREPACK INC.]14Current NDC, Legacy NDC, 10 package rows20250309_102c62ca-da20-4866-84a8-e3513824af4a.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70518-2190-0EA - Each70518-2190b6fab721-38de-48cf-a1aa-b1f5c9bbd74912026-01-08
70518-2190-1EA - Each70518-2190dc54739d-9e6e-469e-8082-8adee5e1abf812026-01-08
70518-2190-2EA - Each70518-21907238c2f1-7aa1-4869-89b5-776bea1e2d0912026-01-08
70518-2190-3EA - Each70518-2190989cfed3-0e5f-4206-97f4-bacd0bdc97a512026-01-08
70518-2190-4EA - Each70518-21908efd7b8a-e169-4021-a191-d6de7b509f0312026-01-08
70518-2190-5EA - Each70518-2190cf968363-6064-434e-9bb9-a0cf8cea9e2512026-01-08

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 34 of 304 · 6,071 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Walgreens VANILLA Hand Sanitizer MistETHYL ALCOHOLWalgreen Company7c083331-3d5f-4248-8b2c-3e7e1b266a792026-06-05WarningsExact identifier
unii: 3K9958V90M
Eryfotona Actinica TintedTITANIUM DIOXIDEISDIN Corp.97357703-0e93-4216-bd1b-a9b2027819592026-06-05WarningsExact identifier
unii: 15FIX9V2JP
GeriGentle Alcohol PadsISOPROPYL ALCOHOLGeri-Gentle Corporation05cda9fa-e503-6e37-e063-6394a90a27112026-06-05WarningsExact identifier
unii: ND2M416302
Signature Series Enriched Foam Alcohol Hand SanitizerALCOHOLCintas3633620e-5057-469c-91a5-c628d1c90aca2026-06-05WarningsExact identifier
unii: 3K9958V90M
VANILLA SCENT HAND SANITIZERETHYL ALCOHOLAmber Glow Cosmetics Limited67c2cb48-481d-41aa-a11d-e00d81d7a34a2026-06-05WarningsExact identifier
unii: 3K9958V90M
Mineral Mattescreen SPF 40 - UntintedTITANIUM DIOXIDE, ZINC OXIDESupergoop, LLC08671d39-3be2-d666-e063-6294a90a62072026-06-04WarningsExact identifier
unii: 15FIX9V2JP
Mineral Mattescreen SPF 40 - Golden HourTITANIUM DIOXIDE, ZINC OXIDESupergoop, LLCc2398820-f003-707f-e053-2a95a90a69292026-06-04WarningsExact identifier
unii: 15FIX9V2JP
GNP Isopropyl Alcohol 70 Percent With Wintergreen OilISOPROPYL ALCOHOLAmerisource Bergen03247512-7a31-4fb4-b7e0-efc337cab6932026-06-04WarningsExact identifier
unii: ND2M416302
Epionce Daily Shield Tinted SPF 50TITANIUM DIOXIDE, ZINC OXIDEEpisciences, Inc.3d1e2921-cba9-4446-e054-00144ff8d46c2026-06-04WarningsExact identifier
unii: 15FIX9V2JP
GNP Isopropyl Rubbing Alcohol 70 PercentISOPROPYL ALCOHOLAmerisource Bergen0ffd9643-3bc2-4b04-92c5-80fe5e429a252026-06-04WarningsExact identifier
unii: ND2M416302
TC Enriched Foam Alcohol Hand SanitizerALCOHOLRubbermaid Commercial Products LLC4f3f0d3f-39c6-4ad4-9cb0-6e0d7b568e512026-06-04WarningsExact identifier
unii: 3K9958V90M
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
OP First Aid Series Insect Sting Relief PadBENZOCAINE, ISOPROPYL ALCOHOLYiwu Ori-Power Medtech Co.,Ltd.b43af183-834a-0f64-e053-2995a90a32182026-06-03WarningsExact identifier
unii: ND2M416302
STRAWBERRY SCENT HAND SANITIZERETHYL ALCOHOLAmber Glow Cosmetics Limited8c9ddf82-fcc8-4575-8a3a-ce11542c3ab42026-06-03WarningsExact identifier
unii: 3K9958V90M
WATERMELON SCENT HAND SANITIZERETHYL ALCOHOLAmber Glow Cosmetics Limitedf49efe3b-5ad7-4658-a1a7-1e46f48d17842026-06-03WarningsExact identifier
unii: 3K9958V90M
CUPCAKE SCENT HAND SANITIZERETHYL ALCOHOLAmber Glow Cosmetics Limitedd1d92aa2-23e6-4c0f-a3da-e00536b606752026-06-03WarningsExact identifier
unii: 3K9958V90M
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
OptiSource Sterile Alcohol Prep PadsISOPROPYL ALCOHOL7051395 Canada Ince49c9ddf-7743-443e-ba85-ee90785f0c722026-06-02WarningsExact identifier
unii: ND2M416302

Reported adverse events (FAERS/openFDA)#

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