Reboost

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Reboost
Generic name: ACONITUM NAPELLUS, BRYONIA ALBA ROOT, EUPATORIUM PERFOLIATUM FLOWERING TOP, GOLDENSEAL, LACHESIS MUTA VENOM, PHOSPHORUS, VINCETOXICUM HIRUNDINARIA ROOT, ZINC GLUCONATE, ZINC ACETATE ANHYDROUS, CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE, IPECAC, SULFUR
Manufacturer: MediNatura Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 781c1a63-5210-4069-8427-bc7df68d6d63
SPL ID: 8b49b20a-1ee8-4625-8c04-280c39ef2197
Version: 2
Effective date: 2023-06-05
Source export date: 2026-10-12
Source partition: 14
Source file: https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/acb9b4700b9af1bdda1c389c7b35bfe38fd6d1a62aa48d17832812be4029b84f/drug-label-0014-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 03:13:02

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 20 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Reboost	openfda.brand_name
generic name		ACONITUM NAPELLUS, BRYONIA ALBA ROOT, EUPATORIUM PERFOLIATUM FLOWERING TOP, GOLDENSEAL, LACHESIS MUTA VENOM, PHOSPHORUS, VINCETOXICUM HIRUNDINARIA ROOT, ZINC GLUCONATE, ZINC ACETATE ANHYDROUS, CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE, IPECAC, SULFUR	openfda.generic_name
manufacturer name		MediNatura Inc.	openfda.manufacturer_name
ndc	package	62795-1044-2	openfda.package_ndc
ndc	product	62795-1044	openfda.product_ndc
ndc11	package	62795104402	derived:openfda.package_ndc
spl id		8b49b20a-1ee8-4625-8c04-280c39ef2197	id
spl set id		781c1a63-5210-4069-8427-bc7df68d6d63	set_id
unii		27YLU75U4W	openfda.unii
unii		ZW3Z11D0JV	openfda.unii
unii		62I3C8233L	openfda.unii
unii		T7J046YI2B	openfda.unii
unii		70FD1KFU70	openfda.unii
unii		RN2HC612GY	openfda.unii
unii		VSW71SS07I	openfda.unii
unii		U0NQ8555JD	openfda.unii
unii		1W0775VX6E	openfda.unii
unii		U6WSN5SQ1Z	openfda.unii
unii		H2ZEY72PME	openfda.unii
unii		9R858U917W	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings: If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If symptoms persist or worsen, a health professional should be consulted. Do not use if known sensitivity to ReBoostTM or any of its ingredients exists.

Reported adverse events (FAERS/openFDA)#

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