ALLERGY RELIEF- onion, apis mellifera, drosera rotundifolia, euphrasia stricta, urtica urens pellet

Allergy Relief by

Drug Labeling and Warnings

Allergy Relief by is a Homeopathic medication manufactured, distributed, or labeled by Homeocare Laboratories. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients:

Allium Cepa 8X, Apis Mel 8X, Drosera 8X, Euphrasia 8X, Histanium 8X, Urtica Urens 8X.

Inactive Ingredients:

Sucrose/lactose.

Purpose:

Temporarily relieves sneezing, coughing, runny nose, nasal congestion, itchy watery eyes and swelling.

Keep out of reach of children.

Keep out of reach of children.

Indications & Usage:

Turn tube upside down, twist cap to break seal & release pellets. Using clear cap, place 3 pellets to

Warnings:

If symptoms persist or worsen, or if pregnant or nursing, consult a doctor. Keep out of reach of children. Do not use if cap seal is broken or missing.

Dosage & Administration:

Turn tube upside down, twist cap to break seal & release pellets. Using clear cap, place 3 pellets to dissolve under your tongue 3 times a day or as needed.

Allergy Relief

Allergy Relief

Homeopathic Medicine

85 Pellets

allergy relief

INGREDIENTS AND APPEARANCE

ALLERGY RELIEF 
onion, apis mellifera, drosera rotundifolia, euphrasia stricta, urtica urens pellet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 61727-301
Route of Administration	SUBLINGUAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ONION (UNII: 492225Q21H) (ONION - UNII:492225Q21H)	ONION	8 [hp_X]  in 4 g
APIS MELLIFERA (UNII: 7S82P3R43Z) (APIS MELLIFERA - UNII:7S82P3R43Z)	APIS MELLIFERA	8 [hp_X]  in 4 g
DROSERA ROTUNDIFOLIA (UNII: QR44N9XPJQ) (DROSERA ROTUNDIFOLIA - UNII:QR44N9XPJQ)	DROSERA ROTUNDIFOLIA	8 [hp_X]  in 4 g
EUPHRASIA STRICTA (UNII: C9642I91WL) (EUPHRASIA STRICTA - UNII:C9642I91WL)	EUPHRASIA STRICTA	8 [hp_X]  in 4 g
URTICA URENS (UNII: IHN2NQ5OF9) (URTICA URENS - UNII:IHN2NQ5OF9)	URTICA URENS	8 [hp_X]  in 4 g

Inactive Ingredients
Ingredient Name	Strength
SUCROSE (UNII: C151H8M554)
LACTOSE (UNII: J2B2A4N98G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 61727-301-21	4 g in 1 TUBE; Type 0: Not a Combination Product	06/08/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		06/08/2012

Labeler - Homeocare Laboratories (088248828)

Registrant - Homeocare Laboratories (088248828)

Establishment
Name	Address	ID/FEI	Business Operations
Homeocare Laboratories		088248828	manufacture(61727-301)