DR TALBOTS INFANT DAILY ALLERGY RELIEF- allium cepa 12x,aralia racemosa 12x,euphrasia officinalis 12x,galphimia glauca 12x,histaminum hydrochloricum 12x,luffa operculata 12x,pulsatilla 12x,solidago 12x,natrum muriaticum 6x liquid

Dr Talbots Infant Daily Allergy Relief by

Drug Labeling and Warnings

Dr Talbots Infant Daily Allergy Relief by is a Homeopathic medication manufactured, distributed, or labeled by Talbot's Pharmaceuticals Family Products,LLC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

Active ingredients (HPUS)

Allium cepa 12X
Aralia racemosa 12X
Euphrasia officinalis 12X.
Galphimia glauca 12X
Histaminum hydrochloricum 12X
Luffa operculata 12X
Pulsatilla 12X
Solidago 12X

CELL SALTS

Natrum muriaticum 6X

INACTIVE INGREDIENTS

Inactive ingredients
Citric acid, glycerin, grape juice, potassium
sorbate, purified water

PURPOSE

Temporarily Relieves:

• Hay Fever
• Sneezing
• Mild wheezing
• Itchy Nose, Thorat, & Watery Eyes
• Runny & Stuffy Nose
  

PREGNANCY

If pregnant or breastfeeding, consult your doctor before use.
Keep out of reach of children.

DIRECTIONS

For sudden onset of symptoms:
Use every 15 minutes for up to
8 doses until symptoms relieved,
then every 2 hours thereafter.

Children
6 - 18 lbs
or 3 - 8 kgs
1.25 mL every 2 hours,
reduce frequency when
symptoms improve

Children

19 - 29 lbs
or 9 - 13 kg

2.5 mL every 2 hours,
reduce frequency when
symptoms improve

Children
30 - 90 lbs
or 14 - 41 kgs

5 mL every 2 hours,
reduce frequency when
symptoms improve

QUESTIONS

Questions or comments?
Call us at 1-855-366-7755 (U.S.A. only)
M-F 8am-5pm CST

ASK A DOCTOR

Ask a doctor before use if you are taking a prescription drug or have a serious medical condition.

Please consult your physician immidiately for a worsening condition.

Warnings

Warnings:

Do not use:

• to treat food allergies
• for persistent or chronic cough
• for treating cough from asthma, smoking, or emphysema
• for treating cough with excessive mucus

A persistent cough may be a sign of a serious condition.

Uses

Temporrarily relieves the symptoms asscociated with hay fever or other upper respiratory allergies, such as

• itchy nose and throat
• watery eyes
• runny nose
• sneezing
• sinus pain
• mild wheezing
  

Keep Out of Reach of Children

Keep out of reach of children.

In case of overdose (or accidental ingestion), get medical help or contact a Poison Control center right away.

DO NOT USE IF SEAL UNDER CAP IS BROKEN OR MISSING.

PRINCIPAL DISPLAY

PRINCIPAL DISPLAY

INGREDIENTS AND APPEARANCE

DR TALBOTS INFANT DAILY ALLERGY RELIEF 
allium cepa 12x,aralia racemosa 12x,euphrasia officinalis 12x,galphimia glauca 12x,histaminum hydrochloricum 12x,luffa operculata 12x,pulsatilla 12x,solidago 12x,natrum muriaticum 6x liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70797-322
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ARALIA RACEMOSA ROOT (UNII: T90W4582DU) (ARALIA RACEMOSA ROOT - UNII:T90W4582DU)	ARALIA RACEMOSA ROOT	12 [hp_X]  in 118 mL
EUPHRASIA STRICTA (UNII: C9642I91WL) (EUPHRASIA STRICTA - UNII:C9642I91WL)	EUPHRASIA STRICTA	12 [hp_X]  in 118 mL
LUFFA OPERCULATA FRUIT (UNII: C4MO6809HU) (LUFFA OPERCULATA FRUIT - UNII:C4MO6809HU)	LUFFA OPERCULATA FRUIT	12 [hp_X]  in 118 mL
ONION (UNII: 492225Q21H) (ONION - UNII:492225Q21H)	ONION	12 [hp_X]  in 118 mL
ANEMONE PULSATILLA (UNII: I76KB35JEV) (ANEMONE PULSATILLA - UNII:I76KB35JEV)	ANEMONE PULSATILLA	12 [hp_X]  in 118 mL
HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U) (HISTAMINE - UNII:820484N8I3)	HISTAMINE DIHYDROCHLORIDE	12 [hp_X]  in 118 mL
SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50) (SOLIDAGO VIRGAUREA FLOWERING TOP - UNII:5405K23S50)	SOLIDAGO VIRGAUREA FLOWERING TOP	12 [hp_X]  in 118 mL
GALPHIMIA GLAUCA FLOWERING TOP (UNII: 93PH5Q8M7E) (GALPHIMIA GLAUCA FLOWERING TOP - UNII:93PH5Q8M7E)	GALPHIMIA GLAUCA FLOWERING TOP	12 [hp_X]  in 118 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37)	SODIUM CHLORIDE	6 [hp_X]  in 118 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
WATER (UNII: 059QF0KO0R)
CONCORD GRAPE JUICE (UNII: F7039Q79LP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70797-322-01	1 in 1 CARTON	09/12/2022
1		118 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		09/12/2022

Labeler - Talbot's Pharmaceuticals Family Products,LLC. (078855555)