Rejuvenation Plus

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
Rejuvenation Plus
Generic name
ARALIA QUIN, ARNICA, AVENA, BARYTA CARB, CARDUUS MAR, DNA, HEPAR SUIS, MEDULLA OSSIS SUIS, PANCREAS SUIS, PHOSPHORICUM AC, PITUITARUM POSTERIUM, THUJA OCC
Manufacturer
Eight and Company L.L.C
Product type
HUMAN OTC DRUG
SPL set ID
bdcdee99-c0e8-4b8c-a0cc-009ecb1ddaae
SPL ID
78d84b6c-c0b4-461a-ba86-705033290091
Version
6
Effective date
2025-12-18
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 03:12:54
Harmonized routes table
Harmonized routes
ORAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS: If symptoms persist or worsen, seek advice of physician. If pregnant or breast-feeding, ask a health care professional before use. Keep out of reach of children . Contains alcohol, in case of overdose, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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