Plant 2 Product Allevatio

Manufacturer
BioLyte Laboratories, LLC
Effective date
2021-10-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:33:57

Label at a glance#

ProductPlant 2 Product Allevatio
Active ingredientFRANGULA CALIFORNICA BARK, RUTA GRAVEOLENS FLOWERING TOP, CALENDULA OFFICINALIS FLOWERING TOP, HYPERICUM PERFORATUM, HORSE CHESTNUT, ARNICA MONTANA, CAULOPHYLLUM THALICTROIDES ROOT, BLACK COHOSH, RHODODENDRON TOMENTOSUM LEAFY TWIG
Label structure15 sections

Indications and uses

Uses For temporary relief of occasional: minor aches and pains of muscles and joints associated with simple backache arthritis strains bruises sprains Indications are based on homeopathic materia medica not clinical tests. Indications are based on theories of homeopathy that are not supported by scientific evidence and most modern allopathic medical professionals.

Dosage and administration

Directions: Adults and children 2 years age and older, apply a thin layer of gel on clean skin to cover the affected area. For best results, allow gel to be absorbed into the skin; do not rub in. Apply at the onset of symptoms, or every 15 minutes for the first hour, but not more than 6 times daily. Children under 2 years of age: Consult a doctor.

Storage and handling

Other Information Store in a cool, dry place. Avoid direct sunlight. Tamper-evident for your protection. Use only if safety seal is intact.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients Purpose

All active ingredients are HPUS* & 3X potency.

Aesculus Hipp., Caulophyllum, Cimicifuga

Racemosa, Hypericum, Ledum, Rhamnus Calif,

Ruta Grav...............................................................Topical Analygesics

Arnica Montana......................................................Anti-inflammatory

Calendula...............................................................Relief for bruising and soreness

*HPUS indicates the active ingredients are in the official Homeopathic Pharmacopeia of the United States.

Purpose

OTC - PURPOSE SECTION

Active Ingredients Purpose

All active ingredients are HPUS* & 3X potency.

Aesculus Hipp., Caulophyllum, Cimicifuga

Racemosa, Hypericum, Ledum, Rhamnus Calif,

Ruta Grav...............................................................Topical Analygesics

Arnica Montana......................................................Anti-inflammatory

Calendula...............................................................Relief for bruising and soreness

*HPUS indicates the active ingredients are in the official Homeopathic Pharmacopeia of the United States.

Uses

INDICATIONS & USAGE SECTION

Uses

For temporary relief of occasional:

  • minor aches and pains of muscles and joints associated with
  • simple backache
  • arthritis
  • strains
  • bruises
  • sprains

Indications are based on homeopathic materia medica not clinical tests.

Indications are based on theories of homeopathy that are not supported by scientific evidence and most modern allopathic medical professionals.

Warnings

WARNINGS SECTION

Warnings

For external use only.

Ask a doctor before use if

OTC - ASK DOCTOR SECTION

As a doctor before use if: taking a prescription drug or have a serious medical condition.

When using this product

OTC - WHEN USING SECTION

When using this product: Avoid contact with eyes or mucous membranes

  • Do not use with other ointments, creams or sprays.
  • Do not apply over large areas of the body or bandage
  • Do not use with heating pad or device

Stop use and ask a doctor if

OTC - STOP USE SECTION

Stop use and ask a doctor if: condition worsens, or if symptoms persist for more than seven (7) days, or clear up and reoccur.

Stop use and ask a doctor if

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if: condition worsens, or if symptoms persist for more than seven (7) days, or clear up and reoccur.

If pregnant or breast-feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding: Ask a healthcare professional before use.

Keep out of reach of children:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children: If accidentally swallowed, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions:

  • Adults and children 2 years age and older, apply a thin layer of gel on clean skin to cover the affected area.
  • For best results, allow gel to be absorbed into the skin; do not rub in.
  • Apply at the onset of symptoms, or every 15 minutes for the first hour, but not more than 6 times daily.
  • Children under 2 years of age: Consult a doctor.

Other Information

STORAGE AND HANDLING SECTION

Other Information

  • Store in a cool, dry place.
  • Avoid direct sunlight.
  • Tamper-evident for your protection. Use only if safety seal is intact.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Cannabidiol (CBD), *Caprylyl Glycol, Carbomer, Citric Acid, *Ethylhexylglycerin, *Lauryl Glucoside, *Myristyl, Glucoside, *Polyglyceryl-6-Laurate, Potassium Sorbate, Purified Water, Sodium Hydroxide

*Plant Based Ingredients

Questions or Comments?

OTC - QUESTIONS SECTION

Questions or Comments?

1-833-4-USA-CBD or visit us at LumenCBD.com

Hours of Operations: M-F 8:00a -6:00p (EST)

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PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58368-01958368-019-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 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
f1f3ee91-4c02-5ac9-e053-2a95a90a3137b479ab40-2534-a354-e053-2995a90ae5622023-01-10WarningsExact identifier
spl set id: b479ab40-2534-a354-e053-2995a90ae562

Reported adverse events (FAERS/openFDA)#

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