Recovatone

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2020-05-21
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:29:32

Label at a glance#

ProductRecovatone
Active ingredientGLYCYRRHIZA GLABRA, POTASSIUM CHLORIDE, DIBASIC POTASSIUM PHOSPHATE, IODINE, ZINC GLUCONATE, PHOSPHORUS, CORTICOTROPIN, ASCORBIC ACID, CALCIUM GLUCONATE, ARGININE, CARNITINE, ORNITHINE, MAGNESIUM CHLORIDE, MAGNESIUM GLUCONATE, MANGANESE GLUCONATE, SODIUM CHLORIDE, EPINEPHRINE, COBALTOUS GLUCONATE, COPPER GLUCONATE, CREATINE, GLUTAMINE, LEUCINE, VALINE, POTASSIUM GLUCONATE, SELENIUM DIOXIDE, FERROUS GLUCONATE, BORON, TRIBASIC CALCIUM PHOSPHATE, MOLYBDENUM, NICKEL, SELENIUM, STRONTIUM CARBONATE, VANADIUM, CHROMIUM
Label structure9 sections

Dosage and administration

Adults and children take four droppers full twice a day for stamina building and muscle recovery; best if taken 1/2 hour prior to workout. For more strenuous workouts, dosage may be increased to eight droppers full. 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): 3.81% of Adrenalinum 8X, Ascorbicum Acidum 6X, Boron 12X, Calcarea Phosphorica 12X, Calcium Gluconate 6X, Chromium 14X, Cobalt Gluconate 8X, Copper Gluconate 8X, Creatine 8X, Ferrous Gluconate 10X, Glutamine 8X, L-Arginine 6X, L-Carnitine 6X, L-Leucine 8X, L-Ornithine 6X, L-Valine 8X, Magnesia Muriatica 6X, Molybdenum 12X, Natrum Muriaticum 6X, Niccolum Metallicum 12X, Potassium Gluconate 8X, Selenium Metallicum 12X, Selenium Dioxide 8X, Strontium Carbonicum 12X, Vanadium Metallicum 12X, Zincum Gluconicum 8X; 0.10% of Adrenocorticotrophin 6X, Glycyrrhiza Glabra 1X, Iodium 4X, Kali Muriaticum 2X, Kali Phosphoricum 3X, Magnesium Gluconicum Dihydricum 6X, Manganese Gluconate 6X, Phosphorus 5X, Zincum Gluconicum 4X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve symptoms associated with exertions, such as muscle pain, muscle weakness, trembling of limbs, and cramps.**

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

WARNINGS:

WARNINGS SECTION

If pregnant or breastfeeding, 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 take four droppers full twice a day for stamina building and muscle recovery; best if taken 1/2 hour prior to workout. For more strenuous workouts, dosage may be increased to eight droppers full.

Consult a physician for use in children under 12 years of age.

INDICATIONS:

INDICATIONS & USAGE SECTION

May temporarily relieve symptoms associated with exertions, such as muscle pain, muscle weakness, trembling of limbs, and cramps.**

**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   800.868.8078

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ENERGIQUE

SINCE 1987

HOMEOPATHIC REMEDY

RECOVATONE

4 fl. oz. (120 ml)

RecovatoneRecovatone

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-045144911-0451-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 36 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
12e6b8f2-bec0-4b69-aaef-2c9182693a2799d752b4-22f4-4fe7-8a72-1bc47ef15c3a2020-05-21WarningsExact identifier
spl id: 12e6b8f2-bec0-4b69-aaef-2c9182693a27
spl set id: 99d752b4-22f4-4fe7-8a72-1bc47ef15c3a

Reported adverse events (FAERS/openFDA)#

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