Home NDC 61594-003 Theraworx Relief Muscle Cramp and Spasm Relief
Product NDC 61594-003
11-digit product format 615940003
Labeler code 61594
Product ID 61594-003_1c333cca-11d4-3dc8-e063-6394a90a0ba8
Type HUMAN OTC DRUG
Nonproprietary name MAGNESIUM SULFATE HEPTAHYDRATE
Dosage form AEROSOL, FOAM
Route TOPICAL
Labeler AVADIM HOLDINGS, INC.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2017-07-22
Substance MAGNESIUM SULFATE HEPTAHYDRATE
Active strength 6 [hp_X]/210mL
Pharmacologic classes Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Theraworx Relief Muscle Cramp and Spasm Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MAGNESIUM SULFATE HEPTAHYDRATE 6 [hp_X]/210mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SK47B8698T Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 61594-003-00 Theraworx Relief Muscle Cramp and Spasm Relief 210 mL in 1 BOTTLE AEROSOL, FOAM 210 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 61594-003 THERAWORX RELIEF MUSCLE CRAMP AND SPASM RELIEF (MAGNESIUM SULFATE HEPTAHYDRATE) AEROSOL, FOAM [AVADIM HOLDINGS, INC.] 7 Current NDC, Legacy NDC, 1 package rows 20240703_d87274cf-97b5-4965-9187-caec621e6177.zip
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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 61594-003-00 61594000300 210 mL in 1 BOTTLE (61594-003-00) 210 ml 2017-07-22 0000-00-00 No No Current