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: APIS MELLIFERA, ATROPA BELLADONNA, ZINC GLUCONATE, BAPTISIA TINCTORIA ROOT, ULMUS RUBRA BARK, SULFUR, ZINC ACETATE ANHYDROUS,VINCETOXICUM HIRUNDINARIA ROOT AND CAIRINA MOSCHATA HEART/LIVER
Manufacturer: MediNatura
Product type: HUMAN OTC DRUG
SPL set ID: d26137fa-6916-473a-9518-b0613e5cbcce
SPL ID: 8a18d95c-9b99-4421-ba4b-a9ce7026d331
Version: 4
Effective date: 2022-08-08
Source export date: 2026-10-12
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:59:47

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 · 23 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		ReBoost	openfda.brand_name
generic name		APIS MELLIFERA, ATROPA BELLADONNA, ZINC GLUCONATE, BAPTISIA TINCTORIA ROOT, ULMUS RUBRA BARK, SULFUR, ZINC ACETATE ANHYDROUS,VINCETOXICUM HIRUNDINARIA ROOT AND CAIRINA MOSCHATA HEART/LIVER	openfda.generic_name
manufacturer name		MediNatura	openfda.manufacturer_name
ndc	package	62795-4004-9	openfda.package_ndc
ndc	product	62795-4004	openfda.product_ndc
ndc11	package	62795400409	derived:openfda.package_ndc
spl id		8a18d95c-9b99-4421-ba4b-a9ce7026d331	id
spl set id		d26137fa-6916-473a-9518-b0613e5cbcce	set_id
unii		11E6VI8VEG	openfda.unii
unii		18E7415PXQ	openfda.unii
unii		W2469WNO6U	openfda.unii
unii		ZW3Z11D0JV	openfda.unii
unii		WQZ3G9PF0H	openfda.unii
unii		70FD1KFU70	openfda.unii
unii		RN2HC612GY	openfda.unii
unii		QI7G114Y98	openfda.unii
unii		065C5D077J	openfda.unii
unii		91QY4PXU8Q	openfda.unii
unii		U6WSN5SQ1Z	openfda.unii
unii		5EF0HWI5WU	openfda.unii
unii		7S82P3R43Z	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 Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult a health professional promptly. Do not use more than 2 days. This product contains ethanol and should not be inhaled. In rare cases allergic reactions may occur. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. The use of this a by more than one person may spread infection. If symptoms persist or worsen, a health professional should be consulted. Do not use if known sensitivity to ReBoost™ or any of its ingredients exists.

Reported adverse events (FAERS/openFDA)#

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