FDA.reportPublic FDA data

Equate Muscle Cramp and Spasm Relief

Manufacturer
Walmart, inc
Effective date
2025-12-17
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:36:17

Label at a glance#

ProductEquate Muscle Cramp and Spasm Relief
Active ingredientMAGNESIUM SULFATE HEPTAHYDRATE
Label structure8 sections

Indications and uses

Prevents Cramps and Spasms Releases Muscle Tightness Relieves Muscle Soreness

Dosage and administration

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

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

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

OTC - PURPOSE SECTION

Muscle Soreness Relief

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

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

Stop use

OTC - STOP USE SECTION

Stop use and ask a doctor if unintended effects occur.

Pregnancy or breast feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

OTC - WHEN USING SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

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 INGREDIENT SECTION

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...?

OTC - QUESTIONS SECTION

Questions or Comments?

1-888-287-1915

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130681131071338GTIN-13: 0681131071338
EAN-13: 0681131071338
GTIN-12: 681131071338
UPC-A: 681131071338
GTIN storage (14 digits): 00681131071338		WAL2104050R01_HiRes.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6e3c022f-0786-43f1-8857-edff89d5153fProduct name120260309
95250459-30e4-45c1-b08a-993044f49109Product name220250805
efd58652-cb8f-4018-91ca-4b0eb2ff729fProduct name720240226
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
2641ccb3-721d-4fbf-9f2f-ca2f18157a62Product name320210309
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
e7e58cd3-cacb-49df-8d34-1ee335614abbProduct name120150609
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79903-100-18Equate Muscle Cramp and Spasm Relief100 mL in 1 BOTTLELIQUID1003

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79903-10079903-100-18

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
ALOE VERA LEAFZY81Z83H0XIACT
SILVER3M4G523W1GIACT
GLYCERINPDC6A3C0OXIACT
ASCORBIC ACIDPQ6CK8PD0RIACT
DISODIUM LAURETH SULFOSUCCINATED6DH1DTN7EIACT
MAGNESIUM SULFATE HEPTAHYDRATESK47B8698TACTIB
SODIUM BENZOATEOJ245FE5EUIACT
SODIUM COCOYL ISETHIONATE518XTE8493IACT
TOCOPHEROLR0ZB2556P8IACT
PEG-8 DIMETHICONEGIA7T764ODIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
ALCOHOL3K9958V90MIACT
METHYL GLUCETH-10N0MWT4C7WHIACT
POLYETHYLENE GLYCOL 700762678AC5RIACT
PHENOXYETHANOLHIE492ZZ3TIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
POLYETHYLENE GLYCOL 15001212Z7S33AIACT
SORBIC ACIDX045WJ989BIACT
CAPRYLYL GLYCOL00YIU5438UIACT
SODIUM BICARBONATE8MDF5V39QOIACT

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
Equate Muscle Cramp and Spasm ReliefMAGNESIUM SULFATE HEPTAHYDRATEWalmart, incdd07a317-abc0-18e8-e053-2995a90ae5a92025-12-17WarningsExact identifier
ndc (package): 79903-100-18
ndc (product): 79903-100
ndc11 (package): 79903010018
spl id: 462e8076-724c-ee44-e063-6294a90a8311
spl set id: dd07a317-abc0-18e8-e053-2995a90ae5a9

Reported adverse events (FAERS/openFDA)#

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