ReBoost Immune

Product NDC
62795-1027
Requested package NDC
62795-1027-2
11-digit product format
627951027
Labeler code
62795
Product ID
62795-1027_5d140604-45be-4576-8eb3-bab6440d1c71
Type
HUMAN OTC DRUG
Nonproprietary name
ACONITUM NAPELLUS,CYNANCHUM VINCETOXICUM ROOT, and SULFUR
Dosage form
TABLET
Route
ORAL
Labeler
MediNatura
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2014-09-30
Marketing end
2025-03-31
Substance
ACONITUM NAPELLUS; CYNANCHUM VINCETOXICUM ROOT; SULFUR
Active strength
6 [hp_X]/1; [hp_X]/1; [hp_X]/1
NDC exclude flag
No
Listing certified through
0000-00-00
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 packagepackage62795-102762795-1027-2DDiscontinued by firm2026-10-12

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 packagepackage62795-102762795-1027-2DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage62795-102762795-1027-2DDiscontinued by firmexcluded / ndc_excluded.zipf5e01cc5f278…a2eaf40c39c3…

Reported adverse events (FAERS/openFDA)#

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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
62795-1027-2EA - Each62795-1027dc7e495c-6fdb-4ca4-b773-a23bdfb428af12015-10-02

DailyMed Socrata Ingredients#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
62795-1027-262795102702100 TABLET in 1 PACKAGE (62795-1027-2) 100 tablet2014-09-302025-03-31NoNoCurrent