FDA.reportPublic FDA data

Exoden Cure Powder

Product NDC
70602-004
Requested package NDC
70602-004-04
11-digit product format
706020004
Labeler code
70602
Product ID
70602-004_d9ceb4d2-1f39-f556-e053-2a95a90a8f38
Type
HUMAN OTC DRUG
Nonproprietary name
Aluminum Chlorohydroxy Allantoinate
Dosage form
POWDER
Route
TOPICAL
Labeler
LIFEON Corp.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2021-03-09
Marketing end
0000-00-00
Substance
ALCLOXA
Active strength
0 g/100g
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

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 packagepackage70602-00470602-004-04IInactivated by FDA2026-09-14

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 · 9 matching rows.

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

Captured / source date, Code, Status table
Captured / source dateCodeStatusSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05IInactivated by FDAd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26IInactivated by FDAf5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-31IInactivated by FDA2ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28IInactivated by FDAa1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21IInactivated by FDAcfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10IInactivated by FDAcdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31UExcluded because listing certification expired302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20UExcluded because listing certification expireded331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10UExcluded because listing certification expired0efc9e666f02…f202fb6c5f17…

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70602-004-022025-01-30C16284748780-12cef2736-8f1a-d83d-e063-dadaa90ab31f70602-004_Exoden Cure Powder
70602-004-042025-01-30C16284748780-12cef2736-8f1a-d83d-e063-dadaa90ab31f70602-004_Exoden Cure Powder
70602-004-062025-01-30C16284748780-12cef2736-8f1a-d83d-e063-dadaa90ab31f70602-004_Exoden Cure Powder

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70602-004-01Exoden Cure Powder10 g in 1 POUCHPOWDER102
70602-004-02Exoden Cure Powder1 in 1 CARTONPOWDER12
70602-004-03Exoden Cure Powder30 g in 1 CONTAINERPOWDER302
70602-004-04Exoden Cure Powder1 in 1 CARTONPOWDER12
70602-004-05Exoden Cure Powder70 g in 1 CONTAINERPOWDER702
70602-004-06Exoden Cure Powder1 in 1 CARTONPOWDER12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70602-004EXODEN CURE POWDER (ALUMINUM CHLOROHYDROXY ALLANTOINATE) POWDER [LIFEON CORP.]2Legacy NDC, 6 package rows20220310_510c4df6-c405-4401-8bff-f5728de0fb4c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70602-004-04706020004041 CONTAINER in 1 CARTON (70602-004-04) > 30 g in 1 CONTAINER (70602-004-03) 1 container2021-03-090000-00-00NoNoCurrent