Allergy Escape

Product NDC
71753-2010
11-digit product format
717532010
Labeler code
71753
Product ID
71753-2010_64b91e85-cc1e-4952-ba9e-0facfa25225e
Type
HUMAN OTC DRUG
Nonproprietary name
Euphrasia Officinalis, Kali Muriaticum, Natrum Muriaticum, Sabadilla, Wyethia Helenoides, Kali Iodatum, Naphthalinum, Histaminum Hydrochloricum
Dosage form
LIQUID
Route
ORAL
Labeler
Ratis, LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2018-03-21
Marketing end
2023-04-19
Substance
EUPHRASIA STRICTA; HISTAMINE DIHYDROCHLORIDE; NAPHTHALENE; POTASSIUM CHLORIDE; POTASSIUM IODIDE; SCHOENOCAULON OFFICINALE SEED; SODIUM CHLORIDE; WYETHIA HELENIOIDES ROOT
Active strength
6 [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes
Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71753-2010-17175320100130 mL in 1 BOTTLE, SPRAY (71753-2010-1) 30 ml2018-03-210000-00-00NoNoCurrent