FDA.reportPublic FDA data

ALLERGY MIX Phoenix

Manufacturer
ASN
Effective date
2019-02-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:10:58

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:
Let one tablet dissolve slowly under tongue or
chew, then swallow, up to 6 times daily, or as
directed by a health care professional. Do not
swallow whole. Avoid food and fluids 15 minutes
before and after each use.

INACTIVE INGREDIENT SECTION

Inactive Ingredients
Dextrose USP, Magnesium Stearate, Silicon Dioxide.

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

30 CHEWABLE TABLETS

NDC# 72617-4002-3

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

NDC# 72617-5002-4

1  81163 00008  0

LOT # XXXX

PHX AlrgyMix 30Tab 5002-4PHX AlrgyMix 30Tab 5002-4

res

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72617-5002-42022-07-29C16284748780-1e4f33bdf-acd3-d8a0-e053-dadaa90a6e4eALLERGY MIX Phoenix

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72617-5002-4ALLERGY MIX Phoenix30 in 1 BOTTLETABLET, CHEWABLE301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72617-5002ALLERGY MIX PHOENIX (LOCAL REMEDY PHOENIX) TABLET, CHEWABLE [ASN]1Legacy NDC, 1 package rows20190212_66a881de-4fb7-4bb8-92fa-610ce0fb0eb6.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72617-500272617-5002-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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
DEXTROSEIY9XDZ35W2IACT
MAGNESIUM STEARATE70097M6I30IACT
SILICON DIOXIDEETJ7Z6XBU4IACT

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
1921812e-d7a2-4271-be21-0beb955dc4cc66a881de-4fb7-4bb8-92fa-610ce0fb0eb62019-02-11WarningsExact identifier
spl id: 1921812e-d7a2-4271-be21-0beb955dc4cc
spl set id: 66a881de-4fb7-4bb8-92fa-610ce0fb0eb6

Reported adverse events (FAERS/openFDA)#

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