FDA.reportPublic FDA data

Inflatherm

Product NDC
72835-701
Requested package NDC
72835-701-02
11-digit product format
728350701
Labeler code
72835
Product ID
72835-701_a46631b9-de3b-414d-94ae-c6352f4812c8
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Diclofenac Sodium and Menthol / Camphor Gel
Dosage form
KIT
Labeler
V2 Pharma, LLC
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2024-08-13
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage72835-70172835-701-02DDiscontinued by firm2026-08-17

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 12 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-100efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09557ba5c1ecfa…9c80585c8c6e…

Additional Listing Data#

Finished product
Yes
Brand name base
Inflatherm
Listing expiration
2026-12-31

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
630714Internal RxNorm lookup
855926Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
b62f4306-8dbd-4501-8b1e-9aa78f9aee06Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
111d457e-3138-4512-b0ba-d0cd760c4055Product name320250225
0426261e-1bb9-b78b-abd2-80da765a7e3eProduct name220240513
7b6158ae-c3f4-3d73-c35f-6f5d18b9efd7Product name520240320
0ac2f11f-f58d-baf2-71a0-680993b48a61Product name220231211
855d63c3-b090-4636-8fc7-6d39ad23c44fProduct name120230829
bb58f410-04be-65dd-9211-e89ead899698Product name620230323
0fcbc38a-8b29-3348-1cef-5222ea53484fProduct name420220516
c4e1eedc-aca2-4551-8382-89144ed9d049Product name320220126
8d368a34-1453-43ea-828d-0dbcd72b8794Product name820210622
473d070d-1c38-488e-b991-c4d1bf45aab8Product name120210201
d6bab9d2-edce-a213-4796-226ab15472c3Product name620200616
2487e6ef-d419-42fc-aaf8-7acc805d2370Product name220170718
e071c814-e5e7-e7ed-ec76-428765d9c66bProduct name220151120
93148e06-b8d7-4e6c-853e-62f807d17fbbProduct name120151014
dbb00be6-fb1c-4b0a-a770-31f7e05e247eProduct name120150316

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0228-2551-06Inflatherm60 in 1 BOTTLETABLET, DELAYED RELEASE6075 mg6
61577-3234-5Inflatherm85 g in 1 BOTTLE, PLASTICGEL85 g0.03 g in 1g6
72835-701-02Inflatherm1 in 1 CARTONKIT16

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72835-701-02EA - Each72835-7019ff7d8de-1ba7-4401-a739-858fc76c2adc12019-09-05

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72835-701INFLATHERM (DICLOFENAC SODIUM AND MENTHOL / CAMPHOR GEL) KIT [V2 PHARMA, LLC]6Current NDC, Legacy NDC, 3 package rows20240820_b62f4306-8dbd-4501-8b1e-9aa78f9aee06.zip

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
InflathermDICLOFENAC SODIUM AND MENTHOL / CAMPHOR GELV2 Pharma, LLCb62f4306-8dbd-4501-8b1e-9aa78f9aee062024-08-13Boxed warning, Warnings, Adverse reactionsExact identifier
ndc (package): 72835-701-02
ndc (product): 72835-701
ndc11 (package): 72835070102

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
630714camphor 3 % / menthol 3 % Topical GelPSNb62f4306-8dbd-4501-8b1e-9aa78f9aee066
855926diclofenac sodium 75 MG Delayed Release Oral TabletPSNb62f4306-8dbd-4501-8b1e-9aa78f9aee066
630714camphor 0.03 MG/MG / menthol 0.03 MG/MG Topical GelSCDb62f4306-8dbd-4501-8b1e-9aa78f9aee066
855926diclofenac sodium 75 MG Delayed Release Oral TabletSCDb62f4306-8dbd-4501-8b1e-9aa78f9aee066
630714camphor 3 % / menthol 3 % Topical GelSYb62f4306-8dbd-4501-8b1e-9aa78f9aee066

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
72835-701-02728350701021 KIT in 1 CARTON (72835-701-02) * 60 TABLET, DELAYED RELEASE in 1 BOTTLE (0228-2551-06) * 85 g in 1 BOTTLE, PLASTIC (61577-3234-5) 1 kit2024-08-130000-00-00NoNoCurrent