Home FDA labels dc9cb3f4-8286-48c3-bfa0-0ed53a3840b1 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 SILVER NITRATE,EUPHORBIA RESINIFERA RESIN, CALCIUM SULFIDE, GOLDENSEAL, POTASSIUM DICHROMATE,LUFFA OPERCULATA FRUIT, SODIUM CARBONATE, ECHINACEA UNSPECIFIED, CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE AND PULSATILLA VULGARIS
Manufacturer MediNatura
Product type HUMAN OTC DRUG
SPL set ID cb8a8d2a-d9d2-4a71-9279-c5641a9126c6
SPL ID dc9cb3f4-8286-48c3-bfa0-0ed53a3840b1
Version 4
Effective date 2022-07-19
Source export date 2026-10-12
Source partition 10
Source file https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 02:29:02 Harmonized routes table Harmonized routes NASAL
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 · 18 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name ReBoost openfda.brand_name generic name SILVER NITRATE,EUPHORBIA RESINIFERA RESIN, CALCIUM SULFIDE, GOLDENSEAL, POTASSIUM DICHROMATE,LUFFA OPERCULATA FRUIT, SODIUM CARBONATE, ECHINACEA UNSPECIFIED, CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE AND PULSATILLA VULGARIS openfda.generic_name manufacturer name MediNatura openfda.manufacturer_name ndc package 62795-4005-9 openfda.package_ndc ndc product 62795-4005 openfda.product_ndc ndc11 package 62795400509 derived:openfda.package_ndc spl id dc9cb3f4-8286-48c3-bfa0-0ed53a3840b1 id spl set id cb8a8d2a-d9d2-4a71-9279-c5641a9126c6 set_id unii 1TI1O9028K openfda.unii unii 95IT3W8JZE openfda.unii unii C4MO6809HU openfda.unii unii 4N9P6CC1DX openfda.unii unii ZW3Z11D0JV openfda.unii unii RN2HC612GY openfda.unii unii T4423S18FM openfda.unii unii 45P3261C7T openfda.unii unii I76KB35JEV openfda.unii unii 1MBW07J51Q 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 Warnings: Ask a doctor before use if you have asthma. In rare cases bronchospasm may occur in asthmatic patients. Temporary burning, stinging, sneezing, or increased nasal discharge may occur. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. The use of this dispenser 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.