Home NDC 73002-713 MDFARMA COLD and FLU RELIEF
Product NDC 73002-713
11-digit product format 730020713
Labeler code 73002
Product ID 73002-713_efb74881-c1a4-6f81-e053-2995a90a9105
Type HUMAN OTC DRUG
Nonproprietary name ATROPINE, NAJA NAJA VENOM, MAGNESIUM CHLORIDE, POTASSIUM HYDROXIDE
Dosage form SPRAY
Route NASAL
Labeler Green Earth Health Inc.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2020-09-23
Marketing end 0000-00-00
Substance ATROPINE; MAGNESIUM CHLORIDE; NAJA NAJA VENOM; POTASSIUM HYDROXIDE
Active strength 5 [hp_X]/.2mL; [hp_X]/.2mL; [hp_X]/.2mL; [hp_X]/.2mL
Pharmacologic classes Anticholinergic [EPC], Calculi Dissolution Agent [EPC], Cholinergic Antagonists [MoA], Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA], 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 2023-12-31
Current FDA listing Historical FDA.report record Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
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 73002-713-03 MDFARMA COLD and FLU RELIEF 5 mL in 1 BOTTLE, SPRAY SPRAY 5 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 73002-713 MDFARMA COLD AND FLU RELIEF (ATROPINE, NAJA NAJA VENOM, MAGNESIUM CHLORIDE, POTASSIUM HYDROXIDE) SPRAY [GREEN EARTH HEALTH INC.] 6 Legacy NDC, 1 package rows 20240103_8c2acd62-2f81-4dde-b258-870cd9469f6e.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 73002-713-03 73002071303 5 mL in 1 BOTTLE, SPRAY (73002-713-03) 5 ml 2020-09-23 0000-00-00 No No Current