Home NDC 87752-003-01 Nervionix Pro Magnesium Ice
Product NDC 87752-003
Requested package NDC 87752-003-01
11-digit product format 877520003
Labeler code 87752
Product ID 87752-003_5631a520-7225-b6c8-e063-6294a90a1a87
Type HUMAN OTC DRUG
Nonproprietary name Lidocaine Hydrochloride, Menthol,Magnesium Chloride
Dosage form CREAM
Route TOPICAL
Labeler Micelle Laboratories, Incorporated
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2026-06-25
Substance LIDOCAINE HYDROCHLORIDE; MENTHOL; MAGNESIUM CHLORIDE
Active strength 1; 3.7; 2 g/100mL; g/100mL; g/100mL
Pharmacologic classes Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Local Anesthesia [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 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Nervionix Pro Magnesium Ice
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LIDOCAINE HYDROCHLORIDE 1 g/100mL MENTHOL 3.7 g/100mL MAGNESIUM CHLORIDE 2 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination V13007Z41A Internal UNII lookup L7T10EIP3A Internal UNII lookup 02F3473H9O Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2747156 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 Sample Exclude flag Status 87752-003-01 87752000301 240 mL in 1 JAR (87752-003-01) 240 ml 2026-06-25 No No Current