Back and Neck Rescue

Manufacturer
Peaceful Mountain, Inc. | Apotheca Company
Effective date
2024-06-13
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:00:43

Label at a glance#

ProductBack and Neck Rescue
Active ingredientHYPERICUM PERFORATUM WHOLE, PHYTOLACCA AMERICANA ROOT, GUAIACUM OFFICINALE RESIN, RHODODENDRON TOMENTOSUM LEAFY TWIG, CONIUM MACULATUM FLOWERING TOP
Label structure9 sections

Indications and uses

For the temporary relief of minor symptoms of back and neck discomfort.

Dosage and administration

Apply at least 3 times daily over the affected area. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Hypericum Perforatum 3X, Phytolacca Decandra 3X, Guaiacum 6X, Ledum Palustre 6X, Conium Maculatum 30X.

INDICATIONS

OTC - PURPOSE SECTION

For the temporary relief of minor symptoms of back and neck discomfort.

WARNINGS

WARNINGS SECTION

For external use only. 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. When using this product Do not get into eyes. Stop use and ask a doctor if conditions worsen, symptoms last more than 7 days.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Apply at least 3 times daily over the affected area. Consult a physician for use in children under 12 years of age.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Aloe Vera 10X Concentrate, Arnica Montana, Carbomer, Comfrey (leaf), Edetate Disodium (EDTA), Lavandula Spp., Natural plant extract, PEG-33, PEG-8 Dimethicone and PEG-14. Phenoxyethanol, Caprylyl Glycol and Sorbic Acid, Potassium Sorbate, Purified Water, Sodium Hydroxide Solution, Hypericum Perforatum, Ascorbic Acid, Vitamin E Oil, Salix Alba, Achillea Millefolium.

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 symptoms of back and neck discomfort.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

peaceful mountain

THE HEIGHT OF HEALTH

back and neck rescue

homeopathic gel

formulated in boulder, co

Net wt. 0.25 oz (7

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43846-0015-12024-06-13C16284748780-19d75b9d0-b3b9-f424-e053-dadaa90a57ceDrug Facts
43846-0015-12020-01-31C16284748780-19d75b9d0-b3b9-f424-e053-dadaa90a57ceDrug Facts

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CONIUM MACULATUM FLOWERING TOPACTIVE INGREDIENTQ28R5GF3711
GUAIACUM OFFICINALE RESINACTIVE INGREDIENTN0K2Z502R61
HYPERICUM PERFORATUMACTIVE INGREDIENTXK4IUX8MNB1
LEDUM PALUSTRE TWIGACTIVE INGREDIENT877L01IZ0P1
PHYTOLACCA AMERICANA ROOTACTIVE INGREDIENT11E6VI8VEG1
CONIUM MACULATUM FLOWERING TOPACTIVE MOIETYQ28R5GF3711
GUAIACUM OFFICINALE RESINACTIVE MOIETYN0K2Z502R61
HYPERICUM PERFORATUMACTIVE MOIETYXK4IUX8MNB1
LEDUM PALUSTRE TWIGACTIVE MOIETY877L01IZ0P1
PHYTOLACCA AMERICANA ROOTACTIVE MOIETY11E6VI8VEG1
.ALPHA.-TOCOPHEROLINACTIVE INGREDIENTH4N855PNZ11
ACHILLEA MILLEFOLIUMINACTIVE INGREDIENT2FXJ6SW4PK1
Aloe Vera LeafINACTIVE INGREDIENTZY81Z83H0X1
ARNICA MONTANA FLOWERINACTIVE INGREDIENTOZ0E5Y15PZ1
ASCORBIC ACIDINACTIVE INGREDIENTPQ6CK8PD0R1
CAPRYLYL GLYCOLINACTIVE INGREDIENT00YIU5438U1
COMFREY ROOTINACTIVE INGREDIENTM9VVZ08EKQ1
EDETATE DISODIUMINACTIVE INGREDIENT7FLD91C86K1
HYPERICUM PERFORATUMINACTIVE INGREDIENTXK4IUX8MNB1
LAVANDULA ANGUSTIFOLIA FLOWERINACTIVE INGREDIENT19AH1RAF4M1
OREGANO FLOWERING TOPINACTIVE INGREDIENT7K91ZBK8GJ1
PEG-8 DIMETHICONEINACTIVE INGREDIENTGIA7T764OD1
PHENOXYETHANOLINACTIVE INGREDIENTHIE492ZZ3T1
POLYETHYLENE GLYCOL 1500INACTIVE INGREDIENT1212Z7S33A1
POLYETHYLENE GLYCOL 700INACTIVE INGREDIENT762678AC5R1
POTASSIUM SORBATEINACTIVE INGREDIENT1VPU26JZZ41
SALIX ALBA BARKINACTIVE INGREDIENT205MXS71H71
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 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43846-001543846-0015-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 24 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 · 336 matching rows.

DailyMed ingredient, IID ingredient, UNII table
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.ALPHA.-TOCOPHEROL.ALPHA.-TOCOPHEROLH4N855PNZ1TABLET, EXTENDED RELEASE / ORAL4 mgExact identifier — unii candidate
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PHENOXYETHANOLPHENOXYETHANOLHIE492ZZ3TLOTION / TOPICAL1 %w/wExact identifier — unii candidate
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SORBIC ACIDSORBIC ACIDX045WJ989BTABLET / ORAL10 mgExact identifier — unii candidate
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ASCORBIC ACIDASCORBIC ACIDPQ6CK8PD0RSOLUTION / RESPIRATORY (INHALATION)0.04 %w/wExact identifier — unii candidate
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SORBIC ACIDSORBIC ACIDX045WJ989BTABLET, DELAYED RELEASE / ORAL0.03 mgExact identifier — unii candidate
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SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IPOWDER, FOR SUSPENSION / ORAL9 mgExact identifier — unii candidate
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SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32ISOLUTION / RECTALNAExact identifier — unii candidate
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SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IINJECTION, POWDER, FOR SOLUTION / INTRA-ARTERIALADJ PHExact identifier — unii candidate
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SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IINJECTION / INTERSTITIALADJ PHExact identifier — unii candidate
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SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32ILOTION / TOPICAL21 mgExact 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
edc5d0a0-8c77-487a-a28e-4d33b10b91fd3d54ea1d-5527-4255-9ba2-113857b486472024-06-13WarningsExact identifier
spl id: edc5d0a0-8c77-487a-a28e-4d33b10b91fd
spl set id: 3d54ea1d-5527-4255-9ba2-113857b48647

Reported adverse events (FAERS/openFDA)#

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