ALLERGY MIX Los Angeles

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 Los Angeles
Active ingredientALTERNARIA ALTERNATA, PASSALORA FULVA, OLEA EUROPAEA FLOWER, WHITE MULBERRY, JUNIPERUS ASHEI POLLEN, NERIUM OLEANDER FLOWER, JUNIPERUS SCOPULORUM POLLEN, USTILAGO MAYDIS, HISTAMINE DIHYDROCHLORIDE, SCHOENOCAULON OFFICINALE SEED, 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, Histaminum Hydrochloricum 12X,
Sabadilla 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 –
     Los Angeles

ALLERGY RELIEF

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

NO SIDE EFFECTS

HOMEOPATHIC MEDICINE

120 CHEWABLE TABLETS

NDC# 72617-3003-2

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

1  81163 00012  7

LOT # XXXX

LA Alrgy Lbl 60cc 120Tab 3003-2LA Alrgy Lbl 60cc 120Tab 3003-2

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
72617-3003-22022-07-29C16284748780-1e4f33bdf-9d7a-d8a0-e053-dadaa90a6e4eALLERGY MIX Los Angeles

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72617-3003-2ALLERGY MIX Los Angeles120 in 1 BOTTLETABLET, CHEWABLE1201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72617-3003ALLERGY MIX LOS ANGELES (LOCAL REMEDY LOS ANGELES) TABLET, CHEWABLE [ASN]1Legacy NDC, 1 package rows20190212_06bdaff1-313e-4d40-92e1-425e2336b3c3.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72617-300372617-3003-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

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
c86d3d80-e673-4b48-b49d-9a4b1a9e2c1006bdaff1-313e-4d40-92e1-425e2336b3c32019-02-11WarningsExact identifier
spl id: c86d3d80-e673-4b48-b49d-9a4b1a9e2c10
spl set id: 06bdaff1-313e-4d40-92e1-425e2336b3c3

Reported adverse events (FAERS/openFDA)#

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