Home NDC 61594-021 Theraworx Relief for Foot Cramps Foam
Product NDC 61594-021
11-digit product format 615940021
Labeler code 61594
Product ID 61594-021_fa2372ee-b30f-9ddd-e053-6394a90af5b9
Type HUMAN OTC DRUG
Nonproprietary name MAGNESIUM SULFATE, UNSPECIFIED FORM
Dosage form AEROSOL, FOAM
Route TOPICAL
Labeler AVADIM HOLDINGS, INC.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2022-02-01
Substance MAGNESIUM SULFATE, UNSPECIFIED FORM
Active strength 6 [hp_X]/mL
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 for Foot Cramps Foam
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MAGNESIUM SULFATE, UNSPECIFIED FORM 6 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination DE08037SAB 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 61594-021-00 Theraworx Relief for Foot Cramps Foam 101 mL in 1 BOTTLE AEROSOL, FOAM 101 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 61594-021 THERAWORX RELIEF FOR FOOT CRAMPS FOAM (MAGNESIUM SULFATE, UNSPECIFIED FORM) AEROSOL, FOAM [AVADIM HOLDINGS, INC.] 3 Current NDC, Legacy NDC, 1 package rows 20230426_2f7fe6b7-deb0-4bf7-a8cb-15ae468512da.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 61594-021-00 61594002100 101 mL in 1 BOTTLE (61594-021-00) 101 ml 2022-02-01 0000-00-00 No No Current