FDA.reportPublic FDA data

Pain and Inflammation Relief Foam

Product NDC
43689-0044
11-digit product format
436890044
Labeler code
43689
Product ID
43689-0044_61e91bab-d849-4060-bc2b-c47fd97fe907
Type
HUMAN OTC DRUG
Nonproprietary name
Calendula Officinalis, Croton Tiglium, Natrum Muriaticum, Plantago Major, Rhus Tox, Sarsaparilla (Smilax Regelii)
Dosage form
LIQUID
Route
TOPICAL
Labeler
The Magni Company
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2020-08-03
Marketing end
0000-00-00
Substance
CALENDULA OFFICINALIS FLOWERING TOP; CROTON TIGLIUM SEED; SODIUM CHLORIDE; PLANTAGO MAJOR WHOLE; TOXICODENDRON PUBESCENS LEAF; SMILAX ORNATA ROOT
Active strength
12 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC exclude flag
No
Listing certified through
2021-12-31
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 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct43689-0044DDiscontinued by firm2026-10-05
excluded packagepackage43689-004443689-0044-1DDiscontinued by firm2026-10-05

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 · 2 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproduct43689-0044DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage43689-004443689-0044-1DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…

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
43689-0044-12024-02-13C16284748780-1f386c649-bc0d-0266-e053-dadaa90a7c1aDrug Facts:
43689-0044-12023-01-30C16284748780-1f386c649-bc0d-0266-e053-dadaa90a7c1aDrug Facts:

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43689-0044PAIN AND INFLAMMATION RELIEF FOAM (CALENDULA OFFICINALIS, CROTON TIGLIUM, NATRUM MURIATICUM, PLANTAGO MAJOR, RHUS TOX, SARSAPARILLA (SMILAX REGELII)) LIQUID [THE MAGNI COMPANY]2Legacy NDC20240214_d0346702-c306-44a8-89da-3592e155204f.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43689-0044-143689004401118 mL in 1 BOTTLE, PUMP (43689-0044-1) 118 ml2020-08-030000-00-00NoNoCurrent