CVS FOAMING MUSCLE RELIEF- magnesium sulfate heptahydrate liquid

CVS foaming muscle relief by

Drug Labeling and Warnings

CVS foaming muscle relief by is a Homeopathic medication manufactured, distributed, or labeled by CVS Health. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Magnesium Sulfate (Magnesium Sulphurica) 6x 0.05% HPUS

PURPOSE

Soothes muscle soreness

INDICATIONS & USAGE

Helps ease cramps & spasms

Aids in relaxing tight muscles

Soothes muscle Soreness

WARNINGS

For external use only

if eye contact occurs, rinse thoroughly with water.

When using this product

avoid eye contact

do not store at temperature above 120°F

use only as directed

not for ingestion

Stop use and ask a doctor if unintended effects occur.

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

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

DOSAGE & ADMINISTRATION

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

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CVS FOAMING MUSCLE RELIEF 
magnesium sulfate heptahydrate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59779-541
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MAGNESIUM SULFATE HEPTAHYDRATE (UNII: SK47B8698T) (MAGNESIUM CATION - UNII:T6V3LHY838)	MAGNESIUM SULFATE HEPTAHYDRATE	6 [hp_X]  in 506 mL

Inactive Ingredients
Ingredient Name	Strength
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
WATER (UNII: 059QF0KO0R)
PEG/PPG-20/15 DIMETHICONE (UNII: 06R6X77P9C)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59779-541-05	210 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/06/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		09/06/2022

Labeler - CVS Health (062312574)