Allergy Escape

Product NDC
71753-2013
11-digit product format
717532013
Labeler code
71753
Product ID
71753-2013_56e85885-a836-4a35-af69-831bd90422c7
Type
HUMAN OTC DRUG
Nonproprietary name
Allium Cepa, Euphrasia Officinalis, Kali Iodatum, Naphthalinum, Sabadilla, Urtica Urens, Wyethia Helenioides, Histaminum Hydrochloricum
Dosage form
SPRAY
Route
ORAL
Labeler
Ratis, LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-07-12
Substance
EUPHRASIA STRICTA; HISTAMINE DIHYDROCHLORIDE; NAPHTHALENE; ONION; POTASSIUM IODIDE; SCHOENOCAULON OFFICINALE SEED; URTICA URENS WHOLE; WYETHIA HELENIOIDES ROOT
Active strength
8; 12; 8; 8; 8; 8; 8; 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], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Vegetable Proteins [CS]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Allergy Escape
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ONION8 [hp_X]/mL
EUPHRASIA STRICTA12 [hp_X]/mL
POTASSIUM IODIDE8 [hp_X]/mL
NAPHTHALENE8 [hp_X]/mL
SCHOENOCAULON OFFICINALE SEED8 [hp_X]/mL
URTICA URENS WHOLE8 [hp_X]/mL
WYETHIA HELENIOIDES ROOT8 [hp_X]/mL
HISTAMINE DIHYDROCHLORIDE8 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 8 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
492225Q21HInternal UNII lookup
C9642I91WLInternal UNII lookup
1C4QK22F9JInternal UNII lookup
2166IN72UNInternal UNII lookup
6NAF1689IOInternal UNII lookup
IHN2NQ5OF9Internal UNII lookup
J10PD1AQ0NInternal UNII lookup
3POA0Q644UInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
8bd9b9da-570a-4875-a5de-963155f0f837Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71753-2013-1Allergy Escape30 mL in 1 BOTTLE, SPRAYSPRAY301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71753-2013ALLERGY ESCAPE (ALLIUM CEPA, EUPHRASIA OFFICINALIS, KALI IODATUM, NAPHTHALINUM, SABADILLA, URTICA URENS, WYETHIA HELENIOIDES, HISTAMINUM HYDROCHLORICUM) SPRAY [RATIS, LLC]1Current NDC, 1 package rows20230713_8bd9b9da-570a-4875-a5de-963155f0f837.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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Allergy EscapeALLIUM CEPA, EUPHRASIA OFFICINALIS, KALI IODATUM, NAPHTHALINUM, SABADILLA, URTICA URENS, WYETHIA HELENIOIDES, HISTAMINUM HYDROCHLORICUMRatis, LLC8bd9b9da-570a-4875-a5de-963155f0f8372023-07-12WarningsExact identifier
ndc (product): 71753-2013

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71753-2013-17175320130130 mL in 1 BOTTLE, SPRAY (71753-2013-1) 30 ml2023-07-12NoNoCurrent