FDA.reportPublic FDA data

ImmunoBooster

Manufacturer
Eight and Company L.L.C | King Bio Inc. | Apotheca Company
Effective date
2025-12-18
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 02:36:18

Label at a glance#

ProductImmunoBooster
Active ingredientARSENIC TRIOXIDE, BAPTISIA TINCTORIA ROOT, ECHINACEA, UNSPECIFIED, SUS SCROFA BONE MARROW, MERCURIC CHLORIDE, SULFUR IODIDE, THUJA OCCIDENTALIS LEAFY TWIG
Label structure10 sections

Dosage and administration

Adults and children over 12: 2 sprays into the mouth 3 times per day. Under age 12: consult a health care professional.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Arsenicum alb 200C, Baptisia 4X, Echinacea 4X, Medulla ossis suis 6X, Merc corros 200C, Sulphur iod 200C, thuja occ 200C.

PURPOSE:

OTC - PURPOSE SECTION

Supports the body's own capacity to fight illness and helps to temporarily relieve symptoms associated with weak immune function, including:

  • tendency to develop colds & Flu
  • sluggish recovery from colds & Flu
  • tendency to get sore throats

WARNINGS:

WARNINGS SECTION

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.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults and children over 12: 2 sprays into the mouth 3 times per day.

Under age 12: consult a health care professional.

OTHER INFORMATION:

OTHER SAFETY INFORMATION

Do not use if the transparent seal around spray bottle is broken or missing.

INDICATIONS:

INDICATIONS & USAGE SECTION

Supports the body's own capacity to fight illness and helps to temporarily relieve symptoms associated with weak immune function, including:

° tendency to develop colds & flu

° sluggish recovery from colds & flu

° tendency to get sore throats

° natural

° gluten & lactose free

° no artificial flavors or colors

° no known negative side effects

° no known negative drug interactions

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Non-GMO glycerin v/v, organic alcohol 20% v/v and purified water.

QUESTIONS:

OTC - QUESTIONS SECTION

Mfd. for Eight and Company L.L.C.

Gaithersburg, MD 20879 1.800.377.5787

www.sprayology.com

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 61096-1038-1

sprayology

ImmunoBooster

RESTORES NATURAL DEFENSES

HOMEOPATHIC ORAL SPRAY

1.38 fl.oz (41 ml)

ImmunoBooster LBLImmunoBooster LBL

ImmunoBooster CNTImmunoBooster CNT

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
61096-1038-12023-12-14C16284748780-1ba0f9c33-10a8-a910-e053-dadaa90a0b85ImmunoBooster
61096-1038-12023-01-30C16284748780-1ba0f9c33-10a8-a910-e053-dadaa90a0b85ImmunoBooster
61096-1038-12021-02-15C16284748780-1ba0f9c33-10a8-a910-e053-dadaa90a0b85ImmunoBooster
61096-1038-12021-01-29C16284748780-1ba0f9c33-10a8-a910-e053-dadaa90a0b85ImmunoBooster

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61096-1038-1ImmunoBooster41 mL in 1 BOTTLE, SPRAYLIQUID416
61096-1038-1ImmunoBooster1 in 1 CARTONLIQUID16

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ARSENIC TRIOXIDEACTIVE INGREDIENTS7V92P67HO1
BAPTISIA TINCTORIA ROOTACTIVE INGREDIENT5EF0HWI5WU1
ECHINACEA, UNSPECIFIEDACTIVE INGREDIENT4N9P6CC1DX1
MERCURIC CHLORIDEACTIVE INGREDIENT53GH7MZT1R1
SULFUR IODIDEACTIVE INGREDIENTL6L8KA2AA01
SUS SCROFA BONE MARROWACTIVE INGREDIENTVP2CN2G7Y81
THUJA OCCIDENTALIS LEAFY TWIGACTIVE INGREDIENT1NT28V93971
ARSENIC CATION (3+)ACTIVE MOIETYC96613F5AV1
BAPTISIA TINCTORIA ROOTACTIVE MOIETY5EF0HWI5WU1
ECHINACEA, UNSPECIFIEDACTIVE MOIETY4N9P6CC1DX1
MERCURIC CATIONACTIVE MOIETYED30FJ8Y421
SULFUR IODIDEACTIVE MOIETYL6L8KA2AA01
SUS SCROFA BONE MARROWACTIVE MOIETYVP2CN2G7Y81
THUJA OCCIDENTALIS LEAFY TWIGACTIVE MOIETY1NT28V93971
ALCOHOLINACTIVE INGREDIENT3K9958V90M1
GLYCERININACTIVE INGREDIENTPDC6A3C0OX1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61096-103861096-1038-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
ARSENIC TRIOXIDES7V92P67HOACTIB
BAPTISIA TINCTORIA ROOT5EF0HWI5WUACTIB
ECHINACEA, UNSPECIFIED4N9P6CC1DXACTIB
SUS SCROFA BONE MARROWVP2CN2G7Y8ACTIB
MERCURIC CHLORIDE53GH7MZT1RACTIB
SULFUR IODIDEL6L8KA2AA0ACTIB
THUJA OCCIDENTALIS LEAFY TWIG1NT28V9397ACTIB
GLYCERINPDC6A3C0OXIACT
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 4 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
GLYCERINGLYCERINPDC6A3C0OXLIQUID / ORAL2400 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
GLYCERINGLYCERINPDC6A3C0OXLIQUID / ORAL2400 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates

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
ImmunoBoosterARSENICUM ALB, BAPTISIA, ECHINACEA, MEDULLA OSSIS SUIS, MERC CORROS, SULPHUR IOD, THUJA OCCEight and Company L.L.C2124365e-2f93-4019-bad2-2bf58f2db52e2025-12-18WarningsExact identifier
ndc (package): 61096-1038-1
ndc (product): 61096-1038
ndc11 (package): 61096103801
spl id: edfac2b3-f8d9-40ad-af64-251d0034c775
spl set id: 2124365e-2f93-4019-bad2-2bf58f2db52e

Reported adverse events (FAERS/openFDA)#

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