Vital Immune Booster

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
Vital Immune Booster
Generic name
APIS MELLIFICA, BORAX, CARDUUS MARIANUS, CISTUS CANADENSIS, ECHINACEA (ANGUSTIFOLIA), GALIUM APARINE, HEPAR SUIS, HEPAR SULPHURIS CALCAREUM, HGH, HYPOPHYSIS SUIS, NITRICUM ACIDUM, PHYTOLACCA DECANDRA, SULPHUR IODATUM, THUJA OCCIDENTALIS, THYMUS SUIS
Manufacturer
Liddell Laboratories, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
2950dd59-0633-4c62-9aaa-a808e2dbec65
SPL ID
f8aa2249-56ef-434b-a3cb-a3d76271ccaa
Version
3
Effective date
2024-10-31
Source export date
2026-09-28
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:18:02
Harmonized routes table
Harmonized routes
ORAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS: Do not use if you have ever had an allergic reaction to this product or any of its ingredients. Ask a doctor before use if you have been diagnosed with a condition known to weaken immunity such as HIV, the virus that causes AIDS. Stop use and ask a doctor if symptoms persist for more than 7 days, worsen, or if new symptoms occur. Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away. If pregnant or breast feeding, ask a health professional before using product. Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken. Other information: Store at room temperature.

Reported adverse events (FAERS/openFDA)#

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