FDA.reportPublic FDA data

NDC 70518-2811-00 - Diclofenac Sodium

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
70518-2811
Requested NDC
70518-2811-00
Package NDCs from labels
70518-2811-0, 70518-2811-00
Manufacturer
REMEDYREPACK INC.
Effective date
2026-03-30
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Diclofenac Sodium - REMEDYREPACK INC.REMEDYREPACK INC.2026-03-30HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
EffectiveRelated label
2022-02-04These highlights do not include all the information needed to use DICLOFENAC SODIUM TOPICAL SOLUTION safely and effectively. See full prescribing information for DICLOFENAC SODIUM TOPICAL SOLUTION. DICLOFENAC SODIUM topical solution, for topical use. Initial U.S. Approval: 1988
2022-02-04These highlights do not include all the information needed to use DICLOFENAC SODIUM TOPICAL SOLUTION safely and effectively. See full prescribing information for DICLOFENAC SODIUM TOPICAL SOLUTION. DICLOFENAC SODIUM topical solution, for topical use. Initial U.S. Approval: 1988
2022-01-28These highlights do not include all the information needed to use DICLOFENAC SODIUM TOPICAL SOLUTION safely and effectively. See full prescribing information for DICLOFENAC SODIUM TOPICAL SOLUTION. DICLOFENAC SODIUM topical solution, for topical use. Initial U.S. Approval: 1988
2022-01-28These highlights do not include all the information needed to use DICLOFENAC SODIUM TOPICAL SOLUTION safely and effectively. See full prescribing information for DICLOFENAC SODIUM TOPICAL SOLUTION. DICLOFENAC SODIUM topical solution, for topical use. Initial U.S. Approval: 1988

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70518-2811-0Diclofenac Sodium1 in 1 CARTONSOLUTION110
70518-2811-0Diclofenac Sodium150 mL in 1 BOTTLE, DROPPERSOLUTION15010

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70518-2811DICLOFENAC SODIUM SOLUTION [REMEDYREPACK INC.]7Current NDC, Legacy NDC, 2 package rows20250403_d349d286-b462-4f8f-aa39-6173653175d6.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70518-2811-0ML - Milliliter70518-28113a1f9c28-6866-4224-b1d7-fbc3ad43c5e112026-02-05

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 67 of 183 · 3,648 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Perk Hand Sanitizer with MoisturizersALCOHOLWorklifebrands LLC4846937f-905e-faec-e063-6394a90a77a22026-01-13WarningsExact identifier
unii: 3K9958V90M
Hand SanitizerETHANOLSaraya Healthcare30c68860-c7ff-5dbb-e054-00144ff8d46c2026-01-13WarningsExact identifier
unii: 3K9958V90M
Diclofenac sodiumDICLOFENAC SODIUMAvKARE0416ce03-c345-9d9e-e063-6294a90ad9402026-01-13Boxed warning, Warnings, Adverse reactionsExact identifier
unii: QTG126297Q
Hand SanitizerALCOHOLSaje Natural Business Inc.a70da1c6-4ca6-b801-e053-2a95a90ae1a52026-01-13WarningsExact identifier
unii: 3K9958V90M
Diclofenac SodiumDICLOFENAC SODIUM 1%Asclemed USA, Inc.6952a221-17fd-4592-8edc-ff36997435332026-01-13WarningsExact identifier
unii: QTG126297Q
Smart Care CALMING LAVENDER HAND SANITIZERETHYL ALCOHOLAshtel Studios, Inc.88d45355-3578-42bf-8c22-3efcbb99e59a2026-01-13WarningsExact identifier
unii: 3K9958V90M
Smart Care tokidoki Mermicorno SWEET PEA SCENT HAND SANITIZERETHYL ALCOHOLAshtel Studios Inc.529d13e4-f6b7-4c7a-bb62-094f845b94282026-01-13WarningsExact identifier
unii: 3K9958V90M
Smart Care COCONUT BREEZE HAND SANITIZERETHYL ALCOHOLAshtel Studios, Inc.062fc0fd-a501-411c-baff-0ad4c23cae3e2026-01-13WarningsExact identifier
unii: 3K9958V90M
Smart Care LEMON LIME HAND SANITIZERETHYL ALCOHOLAshtel Studios, Ince503895d-7b23-4865-90b3-5348faffd45c2026-01-13WarningsExact identifier
unii: 3K9958V90M
Aspercreme ArthritisDICLOFENAC SODIUMChattem, Inc.81f78685-c416-48b5-8840-eef03a66bc282026-01-12WarningsExact identifier
unii: QTG126297Q
Instant Hand SanitizerALCOHOLHydrox Laboratoriesa818def4-f6e9-4a97-aa26-b7c082ae8d182026-01-12WarningsExact identifier
unii: 3K9958V90M
Instant Hand SanitizerALCOHOLHydrox Laboratories285505b0-ee49-4d01-9019-1052e2fb19642026-01-12WarningsExact identifier
unii: 3K9958V90M
Instant Hand Sanitizer UnscentedALCOHOLHydrox Laboratoriescd42da2c-0235-4410-945b-baabb5c7931b2026-01-12WarningsExact identifier
unii: 3K9958V90M
Instant Hand SanitizerALCOHOLLTC Products Inc.6c16aeec-bef2-41f1-b22d-ac37c36255622026-01-12WarningsExact identifier
unii: 3K9958V90M
Diclofenac Sodium Delayed ReleaseDICLOFENAC SODIUMREMEDYREPACK INC.14c1b1a1-bc06-4722-9612-e88ae52272bc2026-01-12Boxed warning, Warnings, Adverse reactionsExact identifier
unii: QTG126297Q
Hand Essentials Instant Hand AntisepticETHYL ALCOHOLHu-Friedy Mfg. Co., Inc.a580ebfb-2da9-4a20-9a3c-6244dbb7aef12026-01-12WarningsExact identifier
unii: 3K9958V90M
Epi-Clenz Pure Instant Hand AntisepticETHYL ALCOHOLMedline Industries, LP9f2be060-0699-47ab-9398-efe91eef22672026-01-12WarningsExact identifier
unii: 3K9958V90M
PURELL Advanced Hand Sanitizer be PeacefulALCOHOLGOJO Industries, Inc.45810c51-8738-4b8a-8d8f-46b4b41dbe932026-01-12WarningsExact identifier
unii: 3K9958V90M
PURELL Advanced Hand Sanitizer be VibrantALCOHOLGOJO Industries, Inc.3a991a7f-1289-4aeb-82f9-8cebd6a389b52026-01-12WarningsExact identifier
unii: 3K9958V90M
Purell Advanced RefreshingALCOHOLGOJO Industries, Inc.b1beadc4-5cf4-4e28-90cc-3f9fdc132a902026-01-12WarningsExact identifier
unii: 3K9958V90M

Reported adverse events (FAERS/openFDA)#

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