N12

Manufacturer
Apex Energetics Inc.
Effective date
2025-04-22
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 20:39:34

Label at a glance#

ProductN12 IMMUNOSODE
Active ingredientVISCUM ALBUM FRUITING TOP, GONORRHEAL URETHRAL SECRETION HUMAN, RANCID BEEF, STREPTOCOCCUS PYOGENES, SULFUR, SUS SCROFA SPLEEN, BILBERRY, STAPHYLOCOCCUS EPIDERMIDIS, ARSENIC TRIOXIDE, ECHINACEA PURPUREA, OLEA EUROPAEA FLOWER, TUBERCULIN PURIFIED PROTEIN DERIVATIVE, SALMONELLA ENTERICA ENTERICA SEROVAR TYPHI, VACCINIA VIRUS STRAIN NEW YORK CITY BOARD OF HEALTH LIVE ANTIGEN, SUS SCROFA BONE MARROW, TREPONEMIC SKIN CANKER HUMAN, THUJA OCCIDENTALIS LEAFY TWIG, BAPTISIA TINCTORIA ROOT, ECHINACEA ANGUSTIFOLIA, LEVISTICUM OFFICINALE, STAPHYLOCOCCUS HAEMOLYTICUS, STAPHYLOCOCCUS SIMULANS, BRYONIA ALBA ROOT, ULEX EUROPAEUS FLOWER, LACHESIS MUTA VENOM
Label structure7 sections

Dosage and administration

Adults & children ages 12 years and over: Take 10 drops under the tongue 3-4 times a day, or as directed by your healthcare professional. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients

Arsenicum Album

6X 9X 12X 15X 30X

Baptisia Tinctoria

4X 6X 9X 12X 15X

Bone Marrow Suis

4C 7C

Bryonia

6X 8X 12X 15X 20X 30X

Echinacea Angustifolia

3X 6X 9X

Echinacea Purpurea

3X 6X 9X

European Olive Flower

12X 20X 30X

Gorse Flower

12X 20X 30X

Lachesis Mutus

6X 8X 10X 12X 15X 30X

Levisticum Officinale

3X 6X 9X 12X

Luesinum

12X 15X 20X 30X

Medorrhinum

30X

Pyrogenium

12X 15X 20X 30X

Staphylococcus Epidermidis

12X 15X 20X 30X

Staphylococcus Haemolyticus

12X 15X 20X 30X

Staphylococcus Simulans

12X 15X 20X 30X

Streptococcinum

12X 15X 20X 30X

Sulphur

6X 9X 12X 15X 20X 30X

Sus Scrofa Spleen

4C 7C

Thuja Occidentalis

6X 9X 12X 15X 20X 30X

Tuberculinum

12X 15X 20X 30X

Typhoid Vaccine

12X 15X 18X 20X 30X 60X

Vaccininum

12X 15X 20X 30X

Vaccinium Myrtillus

30X

Viscum Album Fruiting Top

3X 5X 8X 10X 12X

INDICATIONS & USAGE SECTION

Uses:

OTC - PURPOSE SECTION

For temporary relief of minor:

sore throat*

fatigue*

headaches*

cough*

swollen tonsils*

*Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Warnings:

WARNINGS SECTION

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding, ask a health professional before use.

OTHER SAFETY INFORMATION

Do not use if clear seal over the cap is broken or missing.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use and ask a doctor if sore throat, fatigue, headaches, cough, swollen tonsils, or other symptoms do not improve within 7 days or are accompanied by fever.

Directions:

DOSAGE & ADMINISTRATION SECTION

Adults & children ages 12 years and over: Take 10 drops under the tongue 3-4 times a day, or as directed by your healthcare professional. Consult a physician for use in children under 12 years of age.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

alcohol (20% by volume), distilled water

OTC - QUESTIONS SECTION

Distributed by Apex Energetics. Questions?

16592 Hale Ave., Irvine, CA 92606, USA

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FUTUREPLEX® N12

ANTITOX®

IMMUNOSODE™

Homeopathic Formula

Sore Throat* Fatigue*

Headaches* Cough*

1 fl oz (30 mL)

Alcohol 20% by Volume

N1221-0401N1221-0401

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 32 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63479-141263479-1412-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 27 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
351de60b-1c4f-d310-e063-6394a90a35c9ba5fbf07-d92b-2b1d-e053-2995a90a7e522025-05-14WarningsExact identifier
spl set id: ba5fbf07-d92b-2b1d-e053-2995a90a7e52

Reported adverse events (FAERS/openFDA)#

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