FDA.reportPublic FDA data

Upper Resp HP

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2024-10-31
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:28:42

Label at a glance#

ProductUpper Resp HP
Active ingredientACTIVATED CHARCOAL, COPPER, DROSERA ROTUNDIFOLIA WHOLE, CALCIUM SULFIDE, IPECAC, LACHESIS MUTA VENOM, LOBELIA INFLATA WHOLE, PHOSPHORUS, PULSATILLA PRATENSIS WHOLE, RUMEX CRISPUS ROOT, SPONGIA OFFICINALIS SKELETON, ROASTED
Label structure9 sections

Dosage and administration

Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

(in each drop): 9.09% of Carbo Vegetabilis 30X, Cuprum Metallicum 30X, Drosera (Rotundifolia) 30X, Hepar Sulphuris Calcareum 30X, Ipecacuanha 30X, Lachesis Mutus 30X, Lobelia Inflata 30X, Phosphorus 30X, Pulsatilla (Pratensis) 30X, Rumex Crispus 30X, Spongia Tosta 30X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve symptoms of chronic cough, heaviness in chest, and bronchial irritation.**

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

WARNINGS:

WARNINGS SECTION

If pregnant or breast-feeding, ask a health 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 a 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

Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

INDICATIONS:

INDICATIONS & USAGE SECTION

May temporarily relieve symptoms of chronic cough, heaviness in chest, and bronchial irritation.**

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

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized water, 20% Ethanol.

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. by Energique, Inc.

201 Apple Blvd

Woodbine, IA 51579 800-869-8078

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ENERGIQUE

SINCE 1987

HOMEOPATHIC REMEDY

UPPER RESP HP

1 fl. oz. (30 ml)

Upper Resp HPUpper Resp HP

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
44911-0595-12024-10-31C16284748780-1f386c64a-2e49-0266-e053-dadaa90a7c1aDRUG FACTS:
44911-0595-12023-01-30C16284748780-1f386c64a-2e49-0266-e053-dadaa90a7c1aDRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0595-1Upper Resp HP30 mL in 1 BOTTLE, DROPPERLIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0595UPPER RESP HP (CARBO VEGETABILIS, CUPRUM METALLICUM, DROSERA (ROTUNDIFOLIA), HEPAR SULPHURIS CALCAREUM, IPECACUANHA, LACHESIS MUTUS, LOBELIA INFLATA, PHOSPHORUS, PULSATILLA (PRATENSIS), RUMEX CRISPUS, SPONGIA TOSTA) LIQUID [ENERGIQUE, INC.]2Current NDC, Legacy NDC, 1 package rows20241102_a9c72c3a-908a-433b-ba9e-4f525b80ecaa.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-059544911-0595-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
ACTIVATED CHARCOAL2P3VWU3H10ACTIB
COPPER789U1901C5ACTIB
DROSERA ROTUNDIFOLIA WHOLEQR44N9XPJQACTIB
CALCIUM SULFIDE1MBW07J51QACTIB
IPECAC62I3C8233LACTIB
LACHESIS MUTA VENOMVSW71SS07IACTIB
LOBELIA INFLATA WHOLE9PP1T3TC5UACTIB
PHOSPHORUS27YLU75U4WACTIB
PULSATILLA PRATENSIS WHOLE8E272251DIACTIB
RUMEX CRISPUS ROOT9N1RM2S62CACTIB
SPONGIA OFFICINALIS SKELETON, ROASTED1PIP394IIDACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

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
Upper Resp HPCARBO VEGETABILIS, CUPRUM METALLICUM, DROSERA (ROTUNDIFOLIA), HEPAR SULPHURIS CALCAREUM, IPECACUANHA, LACHESIS MUTUS, LOBELIA INFLATA, PHOSPHORUS, PULSATILLA (PRATENSIS), RUMEX CRISPUS, SPONGIA TOSTAEnergique, Inc.a9c72c3a-908a-433b-ba9e-4f525b80ecaa2024-10-31WarningsExact identifier
ndc (package): 44911-0595-1
ndc (product): 44911-0595
ndc11 (package): 44911059501
spl id: 95dcbcc9-a898-4bd2-92bc-a8d488664c15
spl set id: a9c72c3a-908a-433b-ba9e-4f525b80ecaa

Reported adverse events (FAERS/openFDA)#

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