Respiforce I Plus

Manufacturer
BioActive Nutritional, Inc. | Apotheca Company
Effective date
2024-10-18
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:28:17

Label at a glance#

ProductRespiforce I Plus
Active ingredientBRYONIA ALBA ROOT, EUPATORIUM PERFOLIATUM FLOWERING TOP, FERROSOFERRIC PHOSPHATE, GELSEMIUM SEMPERVIRENS ROOT, WOOD CREOSOTE, VERATRUM VIRIDE ROOT, CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE
Label structure9 sections

Dosage and administration

10 drops orally, 3 times a day. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Bryonia (Alba) 30C, Eupatorium Perfoliatum 30C, Ferrum Phosphoricum 30C, Gelsemium Sempervirens 30C, Kreosotum 30C, Veratrum Viride 30C, Anas Barbariae, Hepatis ET Cordis Extractum 30C, 200C.

INDICATIONS:

OTC - PURPOSE SECTION

For temporary relief of flu symptoms, fever, chills, body aches and pains.

WARNINGS:

WARNINGS SECTION

If pregnant or breast-feeding, ask a health care professional before use.

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

Do not use if tamper evident seal is broken or missing.

Store in cool, dry place.

KEEP OUT OF REACH OF CHILDREN:

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.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

10 drops orally, 3 times a day. Consult a physician for use in children under 12 years of age.

INDICATIONS:

INDICATIONS & USAGE SECTION

For temporary relief of flu symptoms, fever, chills, body aches and pains.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized Water, 25% Ethanol

QUESTIONS:

OTC - QUESTIONS SECTION

Distributed by:
BioActive Nutritional, Inc.
1803 N. Wickham Rd.
Melbourne, FL 32935
bioactivenutritional.com

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BIOActive Nutritional

RESPIFORCE I PLUS

HOMEOPATHIC

1 FL OZ (30 ml)

Respiforce I PlusRespiforce I Plus

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43857-0598-12024-10-18C16284748780-1f386c64a-2c96-0266-e053-dadaa90a7c1aDRUG FACTS:
43857-0598-12023-01-30C16284748780-1f386c64a-2c96-0266-e053-dadaa90a7c1aDRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43857-0598-1Respiforce I Plus30 mL in 1 BOTTLE, DROPPERLIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43857-0598RESPIFORCE I PLUS (BRYONIA (ALBA), EUPATORIUM PERFOLIATUM, FERRUM PHOSPHORICUM, GELSEMIUM SEMPERVIRENS, KREOSOTUM, VERATRUM VIRIDE, ANAS BARBARIAE, HEPATIS ET CORDIS EXTRACTUM) LIQUID [BIOACTIVE NUTRITIONAL, INC.]2Current NDC, Legacy NDC, 1 package rows20241020_3da3fc7e-eb9c-4cd3-95ee-3250dd90c9c7.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43857-059843857-0598-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
Respiforce I PlusBRYONIA (ALBA), EUPATORIUM PERFOLIATUM, FERRUM PHOSPHORICUM, GELSEMIUM SEMPERVIRENS, KREOSOTUM, VERATRUM VIRIDE, ANAS BARBARIAE, HEPATIS ET CORDIS EXTRACTUMBioActive Nutritional, Inc.3da3fc7e-eb9c-4cd3-95ee-3250dd90c9c72024-10-18WarningsExact identifier
ndc (package): 43857-0598-1
ndc (product): 43857-0598
ndc11 (package): 43857059801
spl id: 019f5cd4-fa28-4ce3-a2fc-005a8e2885a1
spl set id: 3da3fc7e-eb9c-4cd3-95ee-3250dd90c9c7

Reported adverse events (FAERS/openFDA)#

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