FDA.reportPublic FDA data

Allergy Bee Gone

Manufacturer
Buzzagogo, Inc | OHM Pharma
Effective date
2022-11-07
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:18:22

Label at a glance#

ProductAllergy Bee Gone
Active ingredientPOTASSIUM DICHROMATE, SCHOENOCAULON OFFICINALE SEED, LUFFA OPERCULATA FRUIT, HISTAMINE DIHYDROCHLORIDE, GALPHIMIA GLAUCA FLOWERING TOP
Label structure15 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Kali Bichromicum 6X...Sinus congestion

Sabadilla 6X...Sneezing, runny nose

Luffa Operculata 6X...Post-nasal drip

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of childrenKeep out of reach of children

OTC - ASK DOCTOR SECTION

Ask Doctor SectionAsk Doctor Section

OTC - PREGNANCY OR BREAST FEEDING SECTION

Pregnancy or Breast Feeding SectionPregnancy or Breast Feeding Section

OTC - PURPOSE SECTION

Purpose SectionPurpose Section

INACTIVE INGREDIENT SECTION

Inactive IngredientsInactive Ingredients

DESCRIPTION SECTION

Overall DescriptionOverall Description

Box Insert Page 1

INSTRUCTIONS FOR USE SECTION

Box Insert Page 1Box Insert Page 1

Box Insert Page 2

INSTRUCTIONS FOR USE SECTION

Box Insert Page 2Box Insert Page 2

Dosage & Administration

DOSAGE & ADMINISTRATION SECTION

Dosage and AdministrationDosage and Administration

WARNINGS AND PRECAUTIONS SECTION

Warnings and PrecautionsWarnings and Precautions

INDICATIONS & USAGE SECTION

Indications and UsageIndications and Usage

WARNINGS SECTION

Warnings SectionWarnings Section

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display PanelPrincipal Display Panel

Jar Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Jar LabelJar Label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70449-1001-12024-07-30C16284748780-11030e365-0a91-111a-e063-dadaa90a10e2Allergy Bee Gone
70449-1001-12024-01-30C16284748780-11030e365-0a91-111a-e063-dadaa90a10e2Allergy Bee Gone

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70449-1001-1Allergy Bee Gone1 in 1 BOXLIQUID13
70449-1001-1Allergy Bee Gone10 mL in 1 TUBELIQUID103

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70449-1001ALLERGY BEE GONE (KALI BICHROMICUM 6X, SABADILLA 6X, LUFFA OPERCULATA 6X) LIQUID [BUZZAGOGO, INC]3Legacy NDC, 2 package rows20221108_9bb7f84f-be05-7088-e053-2a95a90a9016.zip

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
70449-100170449-1001-1

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
LAVENDER OILZBP1YXW0H8IACT
LIME OILUZH29XGA8GIACT
WATER059QF0KO0RIACT
ASCORBIC ACIDPQ6CK8PD0RIACT
HONEYY9H1V576FHIACT
POTASSIUM DICHROMATET4423S18FMACTIB
SCHOENOCAULON OFFICINALE SEED6NAF1689IOACTIB
LUFFA OPERCULATA FRUITC4MO6809HUACTIB
HISTAMINE DIHYDROCHLORIDE3POA0Q644UACTIB
GALPHIMIA GLAUCA FLOWERING TOP93PH5Q8M7EACTIB

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
ece63611-9589-6b27-e053-2a95a90afb129bb7f84f-be05-7088-e053-2a95a90a90162022-11-07WarningsExact identifier
spl id: ece63611-9589-6b27-e053-2a95a90afb12
spl set id: 9bb7f84f-be05-7088-e053-2a95a90a9016

Reported adverse events (FAERS/openFDA)#

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