CACTUS

Product NDC
60986-1028
11-digit product format
609861028
Labeler code
60986
Product ID
60986-1028_dd1e5aa6-a476-edca-e053-2995a90acca8
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Crataegus laevigata, Cactus grandiflorus, convallaria majalis, camphor, kalmia latifolia, spigelia anthelmia, Lachesis mutus, Arnica montana, tabacum, glonoinum
Dosage form
LIQUID
Route
ORAL
Labeler
Marco Pharma International LLC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1992-03-01
Marketing end
0000-00-00
Substance
ARNICA MONTANA; CAMPHOR (NATURAL); CONVALLARIA MAJALIS; CRATAEGUS LAEVIGATA WHOLE; KALMIA LATIFOLIA LEAF; LACHESIS MUTA VENOM; NITROGLYCERIN; SELENICEREUS GRANDIFLORUS STEM; SPIGELIA ANTHELMIA; TOBACCO LEAF
Active strength
6 [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Nitrate Vasodilator [EPC], Nitrates [CS], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Vasodilation [PE]
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 · 3 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct60986-1028IInactivated by FDA2026-09-14
excluded packagepackage60986-102860986-1028-3DDiscontinued by firm2026-09-14
excluded packagepackage60986-102860986-1028-4IInactivated 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 · 12 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCCodeStatusSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage60986-1028-3DDiscontinued by firmd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage60986-1028-3DDiscontinued by firmf5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-31excluded packagepackage60986-1028-3DDiscontinued by firm2ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28excluded packagepackage60986-1028-3DDiscontinued by firma1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21excluded packagepackage60986-1028-3DDiscontinued by firmcfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10excluded packagepackage60986-1028-3DDiscontinued by firmcdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31excluded packagepackage60986-1028-3DDiscontinued by firm302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20excluded packagepackage60986-1028-3DDiscontinued by firmed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10excluded packagepackage60986-1028-3DDiscontinued by firm0efc9e666f02…f202fb6c5f17…
2020-06-10 20:45 UTC · source 2020-06-10excluded productproductIInactivated by FDA9bebd1f3094a…5416666fcb17…
2020-06-10 20:45 UTC · source 2020-06-10excluded packagepackage60986-1028-3IInactivated by FDA9bebd1f3094a…5416666fcb17…
2020-06-10 20:45 UTC · source 2020-06-10excluded packagepackage60986-1028-4IInactivated by FDA9bebd1f3094a…5416666fcb17…

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7480e90b-004b-ebe4-2243-4f2fefdd9e78Product name220260128
3f158398-73f2-4b90-47d1-5c60e8719a98Product name920250721
ca6149a6-ded3-9f17-6c41-3e88f2c0c9c0Product name220250117
00358076-c817-430b-b924-11d717dc307cProduct name120160718
669af5aa-14f3-3df7-f100-5f580ffd43c1Product name120140508
6ff3bab7-2dce-8bea-d7ce-54687f0c01fbProduct name120140508
8bb82a1c-d0d0-fc27-011f-172e545f0382Product name120140508
cb03406d-e223-80bb-67d8-be80f9b6a4f2Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
60986-1028-32026-01-29Drug Facts
60986-1028-42026-01-29Drug Facts
60986-1028-32020-12-04Drug Facts
60986-1028-42020-12-04Drug Facts
60986-1028-32020-01-31Drug Facts
60986-1028-42020-01-31Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60986-1028-3CACTUS50 mL in 1 BOTTLE, GLASSLIQUID506
60986-1028-4CACTUS100 mL in 1 BOTTLE, GLASSLIQUID1006

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60986-1028CACTUS (CRATAEGUS LAEVIGATA, CACTUS GRANDIFLORUS, CONVALLARIA MAJALIS, CAMPHOR, KALMIA LATIFOLIA, SPIGELIA ANTHELMIA, LACHESIS MUTUS, ARNICA MONTANA, TABACUM, GLONOINUM) LIQUID [MARCO PHARMA INTERNATIONAL LLC.]6Legacy NDC, 2 package rows20241207_7daf5521-8df2-4cf2-b1f6-b46bfad63f67.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
60986-1028-36098610280350 mL in 1 BOTTLE, GLASS (60986-1028-3) 50 ml2018-02-280000-00-00NoNoCurrent
60986-1028-460986102804100 mL in 1 BOTTLE, GLASS (60986-1028-4) 100 ml2018-02-280000-00-00NoNoCurrent