Muscle Ice

Manufacturer
Peaceful Mountain, Inc. | Apotheca Company
Effective date
2022-08-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:55:41

Label at a glance#

ProductMuscle Ice
Active ingredientPHYTOLACCA AMERICANA ROOT, COMFREY ROOT, BELLIS PERENNIS, LEDUM PALUSTRE TWIG, RUTA GRAVEOLENS FLOWERING TOP, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, SILICON DIOXIDE
Label structure9 sections

Indications and uses

For the temporary relief of minor aches and pains of muscles and joints.

Dosage and administration

Adults and children 2 years of age and older. Apply to affected area not more than 3 to 4 times daily, Children under 2 years of age consult doctor.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Phytolacca Decandra 1X, Symphytum Officinale 3X, Bellis Perennis 6X, Ledum Palustre 6X, Ruta Graveolens 6X, Magnesia Phosphorica 9X, Silicea 9X

INDICATIONS

OTC - PURPOSE SECTION

For the temporary relief of minor aches and pains of muscles and joints.

WARNINGS

WARNINGS SECTION

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. 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.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Adults and children 2 years of age and older. Apply to affected area not more than 3 to 4 times daily, Children under 2 years of age consult doctor.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Aloe Vera, Camphor Essential Oil, Carbomer (Ultrez 21), Edetate Disodium, Ginger Essential Oil, Lavender Essential Oil, PEG-33, PEG-8 Dimethicone, PEG-14, Phenoxyethanol, Caprylyl Glycol, Sorbic Acid, Potassium Sorbate, Purified Water, Sodium Hydroxide Solution, St. John's Wort Essential Oil, Vitamin E Oil

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains of muscles and joints.

QUESTIONS

OTC - QUESTIONS SECTION

Dist. by Peaceful Mountain, Inc.

Woodbine, IA  51579

888-303-3388

www.peacefulmountain.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

muscle ice

organic and

wild crafted herbs

peaceful mountain

THE HEIGHT OF HEALTH

homeopathic

pain relieving gel

paraben-free

formulated in

boulder, co

Net wt. 3.7 oz (105 g)

Muscle IceMuscle Ice

Muscle IceMuscle Ice

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43846-0005-12022-08-10C16284748780-19d75b9d1-0b82-f424-e053-dadaa90a57ceDrug Facts
43846-0005-12020-01-31C16284748780-19d75b9d1-0b82-f424-e053-dadaa90a57ceDrug Facts

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
BELLIS PERENNISACTIVE INGREDIENT2HU33I03UY1
COMFREY ROOTACTIVE INGREDIENTM9VVZ08EKQ1
LEDUM PALUSTRE TWIGACTIVE INGREDIENT877L01IZ0P1
MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATEACTIVE INGREDIENTHF539G9L3Q1
PHYTOLACCA AMERICANA ROOTACTIVE INGREDIENT11E6VI8VEG1
RUTA GRAVEOLENS FLOWERING TOPACTIVE INGREDIENTN94C2U587S1
SILICON DIOXIDEACTIVE INGREDIENTETJ7Z6XBU41
BELLIS PERENNISACTIVE MOIETY2HU33I03UY1
COLLOIDAL SILICON DIOXIDEACTIVE MOIETYETJ7Z6XBU41
COMFREY ROOTACTIVE MOIETYM9VVZ08EKQ1
LEDUM PALUSTRE TWIGACTIVE MOIETY877L01IZ0P1
MAGNESIUM CATIONACTIVE MOIETYT6V3LHY8381
PHYTOLACCA AMERICANA ROOTACTIVE MOIETY11E6VI8VEG1
RUTA GRAVEOLENS FLOWERING TOPACTIVE MOIETYN94C2U587S1
.ALPHA.-TOCOPHEROLINACTIVE INGREDIENTH4N855PNZ11
ALOE VERA LEAFINACTIVE INGREDIENTZY81Z83H0X1
CAMPHOR OILINACTIVE INGREDIENT75IZZ8Y7271
CAPRYLYL GLYCOLINACTIVE INGREDIENT00YIU5438U1
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)INACTIVE INGREDIENT59TL3WG5CO1
EDETATE SODIUMINACTIVE INGREDIENTMP1J8420LU1
GINGER OILINACTIVE INGREDIENTSAS9Z1SVUK1
HYPERICUM OILINACTIVE INGREDIENTOZU2FC70HY1
LAVENDER OILINACTIVE INGREDIENTZBP1YXW0H81
MENTHOLINACTIVE INGREDIENTL7T10EIP3A1
PHENOXYETHANOLINACTIVE INGREDIENTHIE492ZZ3T1
POLYETHYLENE GLYCOL 1500INACTIVE INGREDIENT1212Z7S33A1
POLYETHYLENE GLYCOL 400INACTIVE INGREDIENTB697894SGQ1
POLYETHYLENE GLYCOL 700INACTIVE INGREDIENT762678AC5R1
POTASSIUM SORBATEINACTIVE INGREDIENT1VPU26JZZ41
SODIUM HYDROXIDEINACTIVE INGREDIENT55X04QC32I1
SORBIC ACIDINACTIVE INGREDIENTX045WJ989B1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43846-000543846-0005-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 25 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 6 · 308 matching rows.

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SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IINJECTION, SOLUTION / INTRA-ARTICULARADJ PHExact identifier — unii candidate
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SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32ISOLUTION / URETERALADJ PHExact identifier — unii candidate
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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
c9e62b6f-df00-4c98-9be4-f09f4a761ac9a25fa6ee-3238-436d-80ae-17dcfc7bfa0c2022-08-10WarningsExact identifier
spl id: c9e62b6f-df00-4c98-9be4-f09f4a761ac9
spl set id: a25fa6ee-3238-436d-80ae-17dcfc7bfa0c

Reported adverse events (FAERS/openFDA)#

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