Respiforce

Product NDC
43857-0623
11-digit product format
438570623
Labeler code
43857
Product ID
43857-0623_a712f2c0-c148-43a9-a7e6-fb6862968f30
Type
HUMAN OTC DRUG
Nonproprietary name
Carbo Vegetabilis, Cuprum Metallicum, Drosera (Rotundifolia), Ipecacuanha, Lachesis Mutus, Lobelia Inflata, Phosphorus, Pulsatilla (Vulgaris), Rumex Crispus, Spongia Tosta
Dosage form
LIQUID
Route
ORAL
Labeler
BioActive Nutritional, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2022-03-02
Substance
ACTIVATED CHARCOAL; COPPER; DROSERA ROTUNDIFOLIA WHOLE; IPECAC; LACHESIS MUTA VENOM; LOBELIA INFLATA WHOLE; PHOSPHORUS; PULSATILLA VULGARIS WHOLE; RUMEX CRISPUS ROOT; SPONGIA OFFICINALIS SKELETON, ROASTED
Active strength
30; 30; 30; 30; 30; 30; 30; 30; 30; 30 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes
Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Inhibit Ovum Fertilization [PE]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 8 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2024-07-10 04:00 UTC · source 2024-07-09excluded productproduct557ba5c1ecfa…9c80585c8c6e…
2024-07-10 04:00 UTC · source 2024-07-09excluded packagepackage43857-0623-1557ba5c1ecfa…9c80585c8c6e…
2024-05-28 21:12 UTC · source 2024-05-28excluded productproduct8af77b9d5b6f…d9bbb34c5368…
2024-05-28 21:12 UTC · source 2024-05-28excluded packagepackage43857-0623-18af77b9d5b6f…d9bbb34c5368…
2024-05-15 03:39 UTC · source 2024-05-14excluded productproduct834df4deac94…adcc014656a3…
2024-05-15 03:39 UTC · source 2024-05-14excluded packagepackage43857-0623-1834df4deac94…adcc014656a3…
2024-03-11 06:39 UTC · source 2024-03-08excluded productproduct1332a3947898…d4bfe170f9cd…
2024-03-11 06:39 UTC · source 2024-03-08excluded packagepackage43857-0623-11332a3947898…d4bfe170f9cd…

Additional Listing Data#

Finished product
Yes
Brand name base
Respiforce
Brand name suffix
B-HP
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACTIVATED CHARCOAL30 [hp_X]/mL
COPPER30 [hp_X]/mL
DROSERA ROTUNDIFOLIA WHOLE30 [hp_X]/mL
IPECAC30 [hp_X]/mL
LACHESIS MUTA VENOM30 [hp_X]/mL
LOBELIA INFLATA WHOLE30 [hp_X]/mL
PHOSPHORUS30 [hp_X]/mL
PULSATILLA VULGARIS WHOLE30 [hp_X]/mL
RUMEX CRISPUS ROOT30 [hp_X]/mL
SPONGIA OFFICINALIS SKELETON, ROASTED30 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 10 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
2P3VWU3H10Internal UNII lookup
789U1901C5Internal UNII lookup
QR44N9XPJQInternal UNII lookup
62I3C8233LInternal UNII lookup
VSW71SS07IInternal UNII lookup
9PP1T3TC5UInternal UNII lookup
27YLU75U4WInternal UNII lookup
I76KB35JEVInternal UNII lookup
9N1RM2S62CInternal UNII lookup
1PIP394IIDInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
a8308fa0-e11f-45e0-b2bf-2bf1aed5d367Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c599c4a0-705d-4ebb-ab1f-977af038f96aProduct name120251124

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43857-0623-12024-09-12C16284748780-11030e365-6bb7-111a-e063-dadaa90a10e2DRUG FACTS:
43857-0623-12024-01-30C16284748780-11030e365-6bb7-111a-e063-dadaa90a10e2DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43857-0623-1RespiforceB-HP30 mL in 1 BOTTLE, DROPPERLIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43857-0623RESPIFORCE B-HP (CARBO VEGETABILIS, CUPRUM METALLICUM, DROSERA (ROTUNDIFOLIA), IPECACUANHA, LACHESIS MUTUS, LOBELIA INFLATA, PHOSPHORUS, PULSATILLA (VULGARIS), RUMEX CRISPUS, SPONGIA TOSTA) LIQUID [BIOACTIVE NUTRITIONAL, INC.]2Current NDC, Legacy NDC, 1 package rows20240913_a8308fa0-e11f-45e0-b2bf-2bf1aed5d367.zip

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 B-HPCARBO VEGETABILIS, CUPRUM METALLICUM, DROSERA (ROTUNDIFOLIA), IPECACUANHA, LACHESIS MUTUS, LOBELIA INFLATA, PHOSPHORUS, PULSATILLA (VULGARIS), RUMEX CRISPUS, SPONGIA TOSTABioActive Nutritional, Inc.a8308fa0-e11f-45e0-b2bf-2bf1aed5d3672024-09-12WarningsExact identifier
ndc (product): 43857-0623

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43857-0623-14385706230130 mL in 1 BOTTLE, DROPPER (43857-0623-1) 30 ml2022-03-020000-00-00NoNoCurrent