Rescue 5

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2021-06-28
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:14:36

Label at a glance#

ProductRescue 5
Active ingredientCLEMATIS VITALBA FLOWER, HELIANTHEMUM NUMMULARIUM FLOWER, IMPATIENS GLANDULIFERA FLOWER, ORNITHOGALUM UMBELLATUM FLOWERING TOP, PRUNUS CERASIFERA FLOWER
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): 0.10% of Clematis Vitalba (Clematis), Flos 30C, 200C, Helianthemum Nummularium (Rock Rose), Flos 30C, 200C, Impatiens Glandulifera (Impatiens), Flos 30C, 200C, Ornithogalum Umbellatum (Star of Bethlehem), Flos 30C, 200C, Prunus Cerasifera (Cherry Plum), Flos 30C, 200C.

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.

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, 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.

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.

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

RESCUE 5

1 fl. oz. (30 ml)

Rescue 5Rescue 5

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0310-12021-06-28C16284748780-1ba0f9c33-4683-a910-e053-dadaa90a0b85Drug Facts:
44911-0310-12021-01-29C16284748780-1ba0f9c33-4683-a910-e053-dadaa90a0b85Drug Facts:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0310-1Rescue 530 mL in 1 BOTTLE, DROPPERLIQUID303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0310RESCUE 5 (CLEMATIS VITALBA, FLOS, HELIANTHEMUM NUMMULARIUM, FLOS, IMPATIENS GLANDULIFERA, FLOS, ORNITHOGALUM UMBELLATUM, FLOS, PRUNUS CERASIFERA, FLOS) LIQUID [ENERGIQUE, INC.]3Legacy NDC, 1 package rows20210629_d3b6d174-dec8-4643-ba1d-443e663a8736.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-031044911-0310-1

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

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
90889b93-a718-4cd6-a3c4-384c31555680d3b6d174-dec8-4643-ba1d-443e663a87362021-06-28WarningsExact identifier
spl id: 90889b93-a718-4cd6-a3c4-384c31555680
spl set id: d3b6d174-dec8-4643-ba1d-443e663a8736

Reported adverse events (FAERS/openFDA)#

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