Rescue 5

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2024-10-30
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:28:39

Label at a glance#

ProductRescue 5
Active ingredientPRUNUS CERASIFERA FLOWER, CLEMATIS VITALBA FLOWER, IMPATIENS GLANDULIFERA FLOWER, HELIANTHEMUM NUMMULARIUM FLOWER, ORNITHOGALUM UMBELLATUM WHOLE
Label structure9 sections

Dosage and administration

Adults and children 5 to 10 drops orally, 1 time 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): 20% of Clematis Vitalba, Flos 30C, Helianthemum Nummularium, Flos 30C, Impatiens Glandulifera, Flos 30C, Ornithogalum Umbellatum, Flos 30C, Prunus Cerasifera, Flos 30C.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve trauma, terror, panic, tension, fear, and the effects of startling experiences.

**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.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Adults and children 5 to 10 drops orally, 1 time 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.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Demineralized water, 20% Ethanol.

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.

INDICATIONS:

INDICATIONS & USAGE SECTION

May temporarily relieve trauma, terror, panic, tension, fear, and the effects of startling experiences.

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

QUESTIONS

OTC - QUESTIONS SECTION

Dist. by Energique, Inc.

201 Apple Blvd

Woodbine, IA 51579  800.869.8078

PACKAGE DISPLAY LABEL:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ENERGIQUE

SINCE 1987

HOMEOPATHIC REMEDY

RESCUE 5

30C

1 fl. oz. (30 ml)

Rescue 5Rescue 5

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0059-12024-10-30C16284748780-11030e365-6f2d-111a-e063-dadaa90a10e2DRUG FACTS:
44911-0059-12024-01-30C16284748780-11030e365-6f2d-111a-e063-dadaa90a10e2DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0059-1Rescue 530 mL in 1 BOTTLE, DROPPERLIQUID305

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0059RESCUE 5 (CLEMATIS VITALBA, FLOS, HELIANTHEMUM NUMMULARIUM, FLOS, IMPATIENS GLANDULIFERA, FLOS, ORNITHOGALUM UMBELLATUM, FLOS, PRUNUS CERASIFERA, FLOS) LIQUID [ENERGIQUE, INC.]5Current NDC, Legacy NDC, 1 package rows20241101_7e03e008-02a8-408f-9779-b5730e226e74.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CLEMATIS VITALBA FLOWERACTIVE INGREDIENT7SCP4N87CI2
HELIANTHEMUM NUMMULARIUM FLOWERACTIVE INGREDIENT51BRR32WPP2
IMPATIENS GLANDULIFERA FLOWERACTIVE INGREDIENTAJU5O1A5ZV2
ORNITHOGALUM UMBELLATUMACTIVE INGREDIENT9NS3M2Y78S2
PRUNUS CERASIFERA FLOWERACTIVE INGREDIENT0KD7R09EAS2
CLEMATIS VITALBA FLOWERACTIVE MOIETY7SCP4N87CI2
HELIANTHEMUM NUMMULARIUM FLOWERACTIVE MOIETY51BRR32WPP2
IMPATIENS GLANDULIFERA FLOWERACTIVE MOIETYAJU5O1A5ZV2
ORNITHOGALUM UMBELLATUMACTIVE MOIETY9NS3M2Y78S2
PRUNUS CERASIFERA FLOWERACTIVE MOIETY0KD7R09EAS2
ALCOHOLINACTIVE INGREDIENT3K9958V90M2
WATERINACTIVE INGREDIENT059QF0KO0R2

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-005944911-0059-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

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 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
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

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
Rescue 5CLEMATIS VITALBA, FLOS, HELIANTHEMUM NUMMULARIUM, FLOS, IMPATIENS GLANDULIFERA, FLOS, ORNITHOGALUM UMBELLATUM, FLOS, PRUNUS CERASIFERA, FLOSEnergique, Inc.7e03e008-02a8-408f-9779-b5730e226e742024-10-30WarningsExact identifier
ndc (package): 44911-0059-1
ndc (product): 44911-0059
ndc11 (package): 44911005901
spl id: d3f6da1a-61dc-4b91-8473-7ad41cae8738
spl set id: 7e03e008-02a8-408f-9779-b5730e226e74

Reported adverse events (FAERS/openFDA)#

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