POLLEN GUARD WEED MIX WEED POLLEN HAY FEVER SYMPTOM RELIEF - plantago lanceolata liquid

United States - English - NLM (National Library of Medicine)

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Active ingredient:
PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI) (PLANTAGO LANCEOLATA POLLEN - UNII:DO87T1U2CI)
Available from:
Western Allergy Services Ltd.
Administration route:
ORAL
Prescription type:
OTC DRUG
Therapeutic indications:
Hay Fever Symptom Relief temporarily relieves symptoms of hay fever resulting from exposure to weed pollen such as: - runny nose - nasal congestion/pressure - sneezing - itching - water, itchy eyes - hives Stop use and ask a doctor if - condition persists or worsens - mouth, throat, chest or abdominal discomfort occurs - you experience hives, itching, or shortness of breath
Authorization status:
unapproved homeopathic
Authorization number:
76097-004-05

POLLEN GUARD WEED MIX WEED POLLEN HAY FEVER SYMPTOM RELIEF - plantago

lanceolata liquid

Western Allergy Services Ltd.

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for

safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

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English Plantain (Plantago lanceolata) 1X

Hay Fever Symptom Relief

temporarily relieves symptoms of hay fever resulting from exposure to weed pollen such as:

runny nose

nasal congestion/pressure

sneezing

itching

water, itchy eyes

hives

Do not use

if you have asthma, severe immunodeficiencies, malignancies, or autoimmune disease

if you take beta blockers

When using this product

avoid other drugs and medications

avoid food, drink, or teeth brushing for at least 5 minutes after each dose

Stop use and ask a doctor if

condition persists or worsens

mouth, throat, chest or abdominal discomfort occurs

you experience hives, itching, or shortness of breath

If pregnant or breast feeding, ask a health professional before use.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control

Center right away.

Directions

drop of extract may be placed under tongue, retained under the tongue for 2 minutes, then swallowed

adults: take 1 drop (0.05 mL) 2 or 3 times per day before meals

children over 3 years of age: only use treatment regimen if child has experienced more than 6

months of symptoms and is documented for allergies to weed pollen

children under 3 years of age: ask a doctor

Store between 2-8 degrees C

Do not use if safety seal is broken

Glycerin, Water

Questions or Comments?

1-866-335-5294 Monday through Friday 9am-5pm

POLLEN GUARD WEED MIX WEED POLLEN HAY FEVER SYMPTOM RELIEF

plantago lanceolata liquid

Product Information

Product T ype

HUMAN OTC DRUG

Ite m Code (Source )

NDC:76 0 9 7-0 0 4

Route of Administration

ORAL

Active Ingredient/Active Moiety

Ingredient Name

Basis of Strength

Stre ng th

PLANTAGO LANCEO LATA PO LLEN (UNII: DO8 7T1U2CI) (PLANTAGO LANCEOLATA

POLLEN - UNII:DO8 7T1U2CI)

PLANTAGO LANCEOLATA

POLLEN

1 [hp_X]

in 5 mL

Inactive Ingredients

Ingredient Name

Stre ng th

GLYCERIN (UNII: PDC6 A3C0 OX)

WATER (UNII: 0 59 QF0 KO0 R)

Packag ing

#

Item Code

Package Description

Marketing Start Date

Marketing End Date

1

NDC:76 0 9 7-0 0 4-0 5

5 mL in 1 BOTTLE, UNIT-DOSE

Western Allergy Services Ltd.

Marketing Information

Marke ting Cate gory

Application Numbe r or Monograph Citation

Marke ting Start Date

Marke ting End Date

unappro ved ho meo pathic

10 /0 3/20 11

Labeler -

Western Allergy Services Ltd. (208003467)

Registrant -

Western Allergy Services Ltd. (208003467)

Establishment

Name

Ad d re s s

ID/FEI

Busine ss Ope rations

Quantum Allergy Canada, Inc.

246 8 29 324

ma nufa c ture

Revised: 9/2011

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