ALLERGY MIX PHOENIX- local remedy phoenix tablet, chewable

ALLERGY MIX Phoenix by

Drug Labeling and Warnings

ALLERGY MIX Phoenix by is a Homeopathic medication manufactured, distributed, or labeled by ASN. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DRUG FACTS

ACTIVE INGREDIENT

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

PURPOSE

Purpose

Allergy symptom relief

INDICATIONS & USAGE

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

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.

KEEP OUT OF REACH OF CHILDREN

Keep out of the reach of children.

DOSAGE & ADMINISTRATION

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

Inactive Ingredients
Dextrose USP, Magnesium Stearate, Silicon Dioxide.

Principal Display Package

   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

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INGREDIENTS AND APPEARANCE

ALLERGY MIX PHOENIX 
local remedy phoenix tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72617-5002
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H)	ALTERNARIA ALTERNATA	6 [hp_X]
PASSALORA FULVA (UNII: HR6H5057CO) (PASSALORA FULVA - UNII:HR6H5057CO)	PASSALORA FULVA	6 [hp_X]
OLEA EUROPAEA FLOWER (UNII: 498M34P1VZ) (OLEA EUROPAEA FLOWER - UNII:498M34P1VZ)	OLEA EUROPAEA FLOWER	6 [hp_X]
WHITE MULBERRY (UNII: MN25R0HH5A) (WHITE MULBERRY - UNII:MN25R0HH5A)	WHITE MULBERRY	6 [hp_X]
JUNIPERUS ASHEI POLLEN (UNII: 544F8MEY0Y) (JUNIPERUS ASHEI POLLEN - UNII:544F8MEY0Y)	JUNIPERUS ASHEI POLLEN	6 [hp_X]
NERIUM OLEANDER FLOWER (UNII: WO4WVF1WVM) (NERIUM OLEANDER FLOWER - UNII:WO4WVF1WVM)	NERIUM OLEANDER FLOWER	6 [hp_X]
JUNIPERUS SCOPULORUM POLLEN (UNII: 0G82TT8ZFY) (JUNIPERUS SCOPULORUM POLLEN - UNII:0G82TT8ZFY)	JUNIPERUS SCOPULORUM POLLEN	6 [hp_X]
USTILAGO MAYDIS (UNII: 4K7Z7K7SWG) (USTILAGO MAYDIS - UNII:4K7Z7K7SWG)	USTILAGO MAYDIS	6 [hp_X]
CYNODON DACTYLON (UNII: 2Q8MR21NHK) (CYNODON DACTYLON - UNII:2Q8MR21NHK)	CYNODON DACTYLON	12 [hp_X]
AMBROSIA ARTEMISIIFOLIA (UNII: 9W34L2CQ9A) (AMBROSIA ARTEMISIIFOLIA - UNII:9W34L2CQ9A)	AMBROSIA ARTEMISIIFOLIA	12 [hp_X]

Inactive Ingredients
Ingredient Name	Strength
DEXTROSE (UNII: IY9XDZ35W2)
MAGNESIUM STEARATE (UNII: 70097M6I30)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	11mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72617-5002-4	30 in 1 BOTTLE; Type 0: Not a Combination Product	01/23/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		01/23/2019

Labeler - ASN (012050067)

Registrant - ASN (012050067)