FDA.reportPublic FDA data

ALLERGY MIX Phoenix

Manufacturer
ASN
Effective date
2019-01-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:10:54

Label at a glance#

ProductALLERGY MIX Phoenix
Active ingredientALTERNARIA ALTERNATA, PASSALORA FULVA, OLEA EUROPAEA FLOWER, WHITE MULBERRY, JUNIPERUS ASHEI POLLEN, NERIUM OLEANDER FLOWER, JUNIPERUS SCOPULORUM POLLEN, USTILAGO MAYDIS, CYNODON DACTYLON, AMBROSIA ARTEMISIIFOLIA
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients
Alternaria Tenuis 6X, Cladosporium Fulvum 6X,
European Olive 6X, Fruitless Mulberry 6X, Mountain
Cedar 6X, Oleander 6X, Rocky Mountain Juniper 6X,
Ustilago Smut 6X, Bermuda Grass 12X, Ragweed 12X

OTC - PURPOSE SECTION

Purpose

Allergy symptom relief

INDICATIONS & USAGE SECTION

Uses: Allergy symptom relief
For temporary relief of symptoms due to hay fever or other
respiratory allergies. Runny nose, sneezing, irritated eyes,
nasal congestion, itchy nose and throat, sinus pain.

WARNINGS SECTION

Warnings
Children under 12 years of age: consult a physician.
If pregnant or breastfeeding, ask a health care professional
before use. If symptoms persist or worsen consult a
physician.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children.

DOSAGE & ADMINISTRATION SECTION

Directions
Adults & children 12 years of age and older: 10-15 drops
under tongue, up to 6 times daily, or as directed by a health
care professional. Avoid food and fluids 15 minutes before
and after each use.

INACTIVE INGREDIENT SECTION

Inactive Ingredients
20% USP Ethanol, USP Purified Water.

Principal Display Package

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

   ALLERGY MIX™
– LOCAL REMEDY –
       Phoenix

ALLERGY RELIEF

RUNNY NOSE, SNEEZING,
IRRITATED EYES, SINUS
CONGESTION & MORE

NO SIDE EFFECTS

HOMEOPATHIC MEDICINE

NET WT. 1 FL. OZ. (29.6 ML)

NDC# 72617-2002-1

Manufactured for: American Standard Nutraceuticals
Las Vegas, Nevada 89120, allergymix.com 800-959-3796

1  81163 00007  3

LOT # XXXX

PHX AlrgyMix Liquid 2002-1PHX AlrgyMix Liquid 2002-1

res

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72617-2002-12022-07-29C16284748780-1e4f33bdf-9ec0-d8a0-e053-dadaa90a6e4eALLERGY MIX Phoenix

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72617-2002-1ALLERGY MIX Phoenix29.6 mL in 1 BOTTLE, DROPPERLIQUID29.61

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72617-2002ALLERGY MIX PHOENIX (LOCAL REMEDY PHOENIX) LIQUID [ASN]1Legacy NDC, 1 package rows20190129_ea1f1aba-5b56-42d3-bb2b-7480c066b421.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72617-200272617-2002-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALTERNARIA ALTERNATA52B29REC7HACTIB
PASSALORA FULVAHR6H5057COACTIB
OLEA EUROPAEA FLOWER498M34P1VZACTIB
WHITE MULBERRYMN25R0HH5AACTIB
JUNIPERUS ASHEI POLLEN544F8MEY0YACTIB
NERIUM OLEANDER FLOWERWO4WVF1WVMACTIB
JUNIPERUS SCOPULORUM POLLEN0G82TT8ZFYACTIB
USTILAGO MAYDIS4K7Z7K7SWGACTIB
CYNODON DACTYLON2Q8MR21NHKACTIB
AMBROSIA ARTEMISIIFOLIA9W34L2CQ9AACTIB
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT

Source Document#

Source XML

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
2256b1c1-db67-4e6d-a0ea-eef68a036d8cea1f1aba-5b56-42d3-bb2b-7480c066b4212019-01-28WarningsExact identifier
spl id: 2256b1c1-db67-4e6d-a0ea-eef68a036d8c
spl set id: ea1f1aba-5b56-42d3-bb2b-7480c066b421

Reported adverse events (FAERS/openFDA)#

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