FDA.reportPublic FDA data

CVS foaming muscle relief

Manufacturer
CVS Health
Effective date
2024-12-11
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 20:46:56

Label at a glance#

ProductCVS foaming muscle relief
Active ingredientMAGNESIUM SULFATE HEPTAHYDRATE
Label structure7 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Magnesium Sulfate (Magnesium Sulphurica) 6x 0.05% HPUS

OTC - PURPOSE SECTION

Soothes muscle soreness

INDICATIONS & USAGE SECTION

Helps ease cramps & spasms

Aids in relaxing tight muscles

Soothes muscle Soreness

WARNINGS SECTION

For external use only

if eye contact occurs, rinse thoroughly with water.

OTC - WHEN USING SECTION

When using this product

avoid eye contact

do not store at temperature above 120°F

use only as directed

not for ingestion

OTC - STOP USE SECTION

Stop use and ask a doctor if unintended effects occur.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If product is swallowed, get medical help or contact poison Control Center right away

DOSAGE & ADMINISTRATION SECTION

Directions

Shake well

apply 2 pumps onto entire muscle group(s) or area

briskly rub in until absorbed

use as needed

allow to air dry

INACTIVE INGREDIENT SECTION

Aloe Vera, Citric Acid, Cocamidopropyl Betaine, Disodium EDTA, Fragrance, Lauryl Glucoside, PEG/PPG-20/15 Dimethicone, Phenoxyethanol, Polysorbate 80, Purified Water, Vitamin E Acetate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage Label

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59779-541CVS FOAMING MUSCLE RELIEF (MAGNESIUM SULFATE HEPTAHYDRATE) LIQUID [CVS HEALTH]3Legacy NDC20241213_c7435d36-fddf-3abb-e053-2a95a90a28a4.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59779-54159779-541-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
WATER059QF0KO0RIACT
PEG/PPG-20/15 DIMETHICONE06R6X77P9CIACT
POLYSORBATE 806OZP39ZG8HIACT
ALOE VERA LEAFZY81Z83H0XIACT
MAGNESIUM SULFATE HEPTAHYDRATESK47B8698TACTIB
PHENOXYETHANOLHIE492ZZ3TIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
LAURYL GLUCOSIDE76LN7P7UCUIACT

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
471acaac-4f76-ac85-e063-6294a90a1683c7435d36-fddf-3abb-e053-2a95a90a28a42025-12-29WarningsExact identifier
spl set id: c7435d36-fddf-3abb-e053-2a95a90a28a4

Reported adverse events (FAERS/openFDA)#

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