Allergy Escape

Product NDC
71753-2012
11-digit product format
717532012
Labeler code
71753
Product ID
71753-2012_53a04308-e36f-420f-88fa-6ebbebaf106c
Type
HUMAN OTC DRUG
Nonproprietary name
Allium Cepa, Apis Mellifica, Euphrasia Officinalis, Kali Iodatum, Naphthalinum, Sabadilla, Wyethia Helenoides, Histaminum Hydrochloricum
Dosage form
LIQUID
Route
ORAL
Labeler
Ratis, LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2019-04-10
Marketing end
2025-06-03
Substance
APIS MELLIFERA; EUPHRASIA STRICTA; HISTAMINE DIHYDROCHLORIDE; NAPHTHALENE; ONION; POTASSIUM IODIDE; SCHOENOCAULON OFFICINALE SEED; WYETHIA HELENIOIDES ROOT
Active strength
8 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes
Allergens [CS], Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Standardized Insect Venom Allergenic Extract [EPC], Vegetable Proteins [CS]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct71753-2012DDiscontinued by firm2026-10-05
excluded packagepackage71753-201271753-2012-1DDiscontinued by firm2026-10-05

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 4 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproductd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage71753-2012-1d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage71753-2012-1f5e01cc5f278…a2eaf40c39c3…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71753-2012ALLERGY ESCAPE (ALLIUM CEPA, APIS MELLIFICA, EUPHRASIA OFFICINALIS, KALI IODATUM, NAPHTHALINUM, SABADILLA, WYETHIA HELENOIDES, HISTAMINUM HYDROCHLORICUM) LIQUID [RATIS, LLC]3Legacy NDC20220309_662b8831-ab56-4058-b76d-0a8f548920e0.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71753-2012-17175320120130 mL in 1 BOTTLE, SPRAY (71753-2012-1) 30 ml2019-04-102025-06-03NoNoCurrent