Home NDC 68703-352 TremorSoothe
Product NDC 68703-352
11-digit product format 687030352
Labeler code 68703
Product ID 68703-352_2ab1287c-c753-6a71-e063-6394a90a1cdd
Type HUMAN OTC DRUG
Nonproprietary name Agaricus musc, Mag phos, Stramonium, Tarentula hisp
Dosage form TABLET
Route ORAL
Labeler Silver Star Brands
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2020-12-25
Substance AMANITA MUSCARIA FRUITING BODY; DATURA STRAMONIUM; LYCOSA TARANTULA; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE
Active strength 6; 6; 6; 8 [hp_C]/1801; [hp_C]/1801; [hp_C]/1801; [hp_X]/1801
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 TremorSoothe
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AMANITA MUSCARIA FRUITING BODY 6 [hp_C]/1801 MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 6 [hp_C]/1801 LYCOSA TARANTULA 6 [hp_C]/1801 DATURA STRAMONIUM 8 [hp_X]/1801
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 68703-352-80 TremorSoothe 189 in 1 BOTTLE, GLASS TABLET 189 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68703-352 TREMORSOOTHE (AGARICUS MUSC, MAG PHOS, STRAMONIUM, TARENTULA HISP) TABLET [SILVER STAR BRANDS] 5 Current NDC, Legacy NDC, 1 package rows 20250103_b6c17f42-6a08-6f89-e053-2a95a90aafaa.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 68703-352-80 68703035280 189 TABLET in 1 BOTTLE, GLASS (68703-352-80) 189 tablet 2020-12-25 0000-00-00 No No Current