EQUATE MUSCLE CRAMP AND SPASM RELIEF- magnesium sulfate heptahydrate liquid

Equate Muscle Cramp and Spasm Relief by

Drug Labeling and Warnings

Equate Muscle Cramp and Spasm Relief by is a Homeopathic medication manufactured, distributed, or labeled by Walmart, inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Contains Magnesium Sulfate (Magnesia sulphurica) 6X 0.05% HPUS

"HPUS" indicates the active ingredient in this product is in the Homeopathic Pharmacopoeia of the United States.

Purpose

Muscle Soreness Relief

Uses

• Prevents Cramps and Spasms
• Releases Muscle Tightness
• Relieves Muscle Soreness

Warnings

For external use only.

When using this product

• Avoid eye contact
• Store between 32°F and 120°F
• Use only as directed
• Not for ingestion

Stop use

Stop use and ask a doctor if unintended effects occur.

Pregnancy or breast feeding

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

Keep out of reach of children.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

When using

USE ONLY AFTER DIAGNOSIS BY A PHYSICIAN AND UNDER THE SUPERVISION OF A PHYSICIAN. If eye contact occurs, rinse with water.

Directions

Directions Shake bottle well Apply 2 pumps on each impacted muscle group. Rub in briskly until absorbed Repeat Allow to air dry Use as needed

Inactive Ingredients

Inactive ingredients

Aloe vera leaf juice, Ascorbic acid, Caprylyl glycol, Citric acid, Cocamidopropyl betaine, Disodium laureth sulfosuccinate, Ethanol, Glycerin, Ionic colloidal silver, Methyl gluceth-10, PEG-8 Dimethicone, PEG-14, PEG-33, Phenoxyethanol, Potassium sorbate, Purified water, Sodium benzoate, Sodium bicarbonate, Sodium cocoyl isethionate, Sorbic acid, Tocopherols (soy)

Questions...?

Questions or Comments?

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FDA Disclaimer: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

INGREDIENTS AND APPEARANCE

EQUATE MUSCLE CRAMP AND SPASM RELIEF 
magnesium sulfate heptahydrate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79903-100
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 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
SILVER (UNII: 3M4G523W1G)
GLYCERIN (UNII: PDC6A3C0OX)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)
TOCOPHEROL (UNII: R0ZB2556P8)
PEG-8 DIMETHICONE (UNII: GIA7T764OD)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
ALCOHOL (UNII: 3K9958V90M)
METHYL GLUCETH-10 (UNII: N0MWT4C7WH)
POLYETHYLENE GLYCOL 700 (UNII: 762678AC5R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A)
SORBIC ACID (UNII: X045WJ989B)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79903-100-18	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/19/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		04/19/2022

Labeler - Walmart, inc (051957769)