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 47 of 301 · 6,019 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
B-Pure Moisturizing Hand Sanitizer Vanilla Creme ScentedALCOHOLFourstar Group USA, Inc.13faded0-7953-4d86-b952-e4bcf4ba53cc2026-04-28WarningsExact identifier
unii: 3K9958V90M
B-Pure Moisturizing Hand Sanitizer Sweet Plum and Jasmine ScentedALCOHOLFourstar Group USA, Inc.450d025a-cc11-796e-e063-6394a90a7e5c2026-04-28WarningsExact identifier
unii: 3K9958V90M
AmoxicillinAMOXICILLINCoupler LLC5037e2a5-52e9-caec-e063-6294a90ad8372026-04-28Warnings, Adverse reactionsExact identifier
rxcui: 308194
unii: 804826J2HU
B-Pure Hand Sanitizer Coconut Vanilla ScentedALCOHOLFourstar Group USA, Inc.e179b21d-fb93-4671-87c0-b8ae094533282026-04-28WarningsExact identifier
unii: 3K9958V90M
Anything SPFOCTINOXATE, OCTISALATE, ZINC OXIDE, AVOBENZONE, HOMOSALATE, TITANIUM DIOXIDEAnything SPF LLC508b8dcb-6600-6dad-e063-6294a90a565a2026-04-28WarningsExact identifier
unii: 15FIX9V2JP
Scriptsusa Hand SanitizerALCOHOLEnergized Solution Corp4f97edd9-717a-315b-e063-6394a90aade72026-04-27WarningsExact identifier
unii: 3K9958V90M
Alcohol wet wipesALCOHOL WET WIPESShandong Aishule Hygiene Products Co., Ltdf79dbac0-cec0-46bc-e053-6294a90a2b132026-04-25WarningsExact identifier
unii: 3K9958V90M
Wet wipesWET WIPESJINGXIN GROUP (M) SDN BHD395225b1-486b-1867-e063-6394a90a18652026-04-25WarningsExact identifier
unii: 3K9958V90M
Hand SanitizerALCOHOLMerchSource, LLC5054a055-50d0-f12a-e063-6294a90ad78e2026-04-25WarningsExact identifier
unii: 3K9958V90M
Amoxicillin and Clavulanate PotassiumAMOXICILLIN AND CLAVULANATE POTASSIUMSportpharm LLCfabeca32-3f26-4b65-b8b6-5f0e23765ab02026-04-24Warnings, Adverse reactionsExact identifier
unii: 804826J2HU
Amoxicillin and Clavulanate PotassiumAMOXICILLIN AND CLAVULANATE POTASSIUMSportpharm LLCcd7d2c0c-bf58-457a-b3d1-bb4c167cd1272026-04-24Warnings, Adverse reactionsExact identifier
unii: 804826J2HU
Ethyl AlcoholETHYL ALCOHOLUpLift Brands, LLC5035ec52-2d65-cbbf-e063-6294a90a4a5c2026-04-24Warnings, Adverse reactionsExact identifier
unii: 3K9958V90M
Foaming Sanitizing HandALCOHOLKutol Products Companyb2e22e51-88f5-4391-8705-3855c1645d802026-04-24WarningsExact identifier
unii: 3K9958V90M
B-Pure Moisturizing Hand Sanitizer Amber Breeze ScentedALCOHOLFourstar Group USA, Inc.eb39678d-7576-4147-be02-b7779a5758282026-04-24WarningsExact identifier
unii: 3K9958V90M
B-Pure Moisturizing Hand Sanitizer Kick Off ScentedALCOHOLFourstar Group USA, Inc.860f25c3-54b0-4438-ba97-0fc81cf350442026-04-24WarningsExact identifier
unii: 3K9958V90M
AmoxicillinAMOXICILLINCoupler LLC5020950a-b248-a463-e063-6294a90ae57f2026-04-23Warnings, Adverse reactionsExact identifier
rxcui: 308191
unii: 804826J2HU
SOUR LEMON HAND SANITIZER Island Coco ScentETHYL ALCOHOLDiamond Life Cosmetics Trading FZCO9e4d9add-0a02-4cce-91e0-7c3ce3ad5cb22026-04-23WarningsExact identifier
unii: 3K9958V90M
SOUR LEMON HAND SANITIZER Sugar Lemon ScentETHYL ALCOHOLDiamond Life Cosmetics Trading FZCObaa5166d-e41f-46aa-adae-038f444bb54e2026-04-23WarningsExact identifier
unii: 3K9958V90M
3M DuraPrep SurgicalIODINE POVACRYLEX AND ISOPROPYL ALCOHOLSolventum US LLC22a10a54-6a04-48b3-9ec4-b26526183daf2026-04-23WarningsExact identifier
unii: ND2M416302
FRESH FEELS HAND SANITIZER MIST LAVENDER SCENTETHYL ALCOHOLAmber Glow Cosmetics Limited8efafedf-a66e-44a3-b2af-700292f1d0012026-04-23WarningsExact identifier
unii: 3K9958V90M

Reported adverse events (FAERS/openFDA)#

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