Muscle Ice

PHYTOLACCA DECANDRA, BELLIS PERENNIS, LEDUM PALUSTRE, RUTA GRAVEOLENS, SYMPHYTUM OFFICINALE, MAGNESIA PHOSPHORICA, SILICEA, MENTHOL (CRYSTALS) TOPICAL HUMAN OTC DRUG

Muscle Ice is an FDA drug label for the active ingredient PHYTOLACCA DECANDRA, BELLIS PERENNIS, LEDUM PALUSTRE, RUTA GRAVEOLENS, SYMPHYTUM OFFICINALE, MAGNESIA PHOSPHORICA, SILICEA, MENTHOL (CRYSTALS) manufactured by Peaceful Mountain, Inc. administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260730.

Generic name
PHYTOLACCA DECANDRA, BELLIS PERENNIS, LEDUM PALUSTRE, RUTA GRAVEOLENS, SYMPHYTUM OFFICINALE, MAGNESIA PHOSPHORICA, SILICEA, MENTHOL (CRYSTALS)
Manufacturer
Peaceful Mountain, Inc.
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
43846-0073
Application
N/A
Label effective
20260730

About this product

Muscle Ice is an FDA-registered drug product whose active ingredient is PHYTOLACCA DECANDRA, BELLIS PERENNIS, LEDUM PALUSTRE, RUTA GRAVEOLENS, SYMPHYTUM OFFICINALE, MAGNESIA PHOSPHORICA, SILICEA, MENTHOL (CRYSTALS). It is labelled by Peaceful Mountain, Inc. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 43846-0073, label effective 20260730. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

What it is used for

Across FDA labelling, products containing PHYTOLACCA DECANDRA, BELLIS PERENNIS, LEDUM PALUSTRE, RUTA GRAVEOLENS, SYMPHYTUM OFFICINALE, MAGNESIA PHOSPHORICA, SILICEA, MENTHOL (CRYSTALS) are most often described in connection with: temporarily relieve, minor aches, pains muscles, joints claims, based traditional, homeopathic principles, accepted medical, fda evaluated. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

ACTIVE INGREDIENTS: (in gel): 4% of Menthol; 0.20% of Bellis 6X, Ledum Palustre 6X, Phytolacca Decandra 4X, Ruta Graveolens 6X, Symphytum Officinale 6X; 0.001% of Magnesia Phosphorica 9X, Silicea 9X.

Indications & Usage

INDICATIONS: May temporarily relieve minor aches and pains of muscles and joints.** **Claims based on traditional homeopathic principles, not accepted medical evidence. Not FDA evaluated.

Dosage & Administration

DIRECTIONS: Adults : Apply to affected area not more than 3 to 4 times daily. Children 2 years of age and older: C onsult a health professional. Do not use on children under 2 years of age.

Warnings

WARNINGS: For external use only. Avoid contact with eyes. If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a doctor. Do not apply to wounds or damaged skin, or mucous membranes. Do not bandage tightly. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. Do not use if saftey seal is broken or missing.

Frequently asked questions

What is Muscle Ice used for?
INDICATIONS: May temporarily relieve minor aches and pains of muscles and joints.** **Claims based on traditional homeopathic principles, not accepted medical evidence. Not FDA evaluated.

Who makes Muscle Ice?
Peaceful Mountain, Inc. is the labeler of record for Muscle Ice.

What form does Muscle Ice come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Muscle Ice prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Has Muscle Ice been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.