Label: ALLERGY RELIEF NOW INHALED ALLERGY REMEDY- inhaled allergy remedy spray
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Contains inactivated NDC Code(s)
NDC Code(s): 61727-052-30 - Packager: Homeocare Laboratories
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
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.
Drug Label Information
Updated March 24, 2014
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- Official Label (Printer Friendly)
- Active Ingredients:
- Inactive Ingredients:
- Suggested Usage:
- PURPOSE
- INDICATIONS & USAGE
- KEEP OUT OF REACH OF CHILDREN
- WARNINGS
- Allergy Now Inhaled Allergy Remedy 1 fl oz
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INGREDIENTS AND APPEARANCE
ALLERGY RELIEF NOW INHALED ALLERGY REMEDY
inhaled allergy remedy sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61727-052 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ONION (UNII: 492225Q21H) (ONION - UNII:492225Q21H) ONION 5 [hp_X] in 1 [hp_X] AMBROSIA ARTEMISIIFOLIA (UNII: 9W34L2CQ9A) (AMBROSIA ARTEMISIIFOLIA - UNII:9W34L2CQ9A) AMBROSIA ARTEMISIIFOLIA 4 [hp_X] in 1 [hp_X] ARUNDO PLINIANA ROOT (UNII: ZXE7LB03WC) (ARUNDO PLINIANA ROOT - UNII:ZXE7LB03WC) ARUNDO PLINIANA ROOT 6 [hp_X] in 1 [hp_X] EUPHRASIA STRICTA (UNII: C9642I91WL) (EUPHRASIA STRICTA - UNII:C9642I91WL) EUPHRASIA STRICTA 3 [hp_X] in 1 [hp_X] HISTAMINE (UNII: 820484N8I3) (HISTAMINE - UNII:820484N8I3) HISTAMINE 12 [hp_X] in 1 [hp_X] NAPHTHALENE (UNII: 2166IN72UN) (NAPHTHALENE - UNII:2166IN72UN) NAPHTHALENE 5 [hp_X] in 1 [hp_X] SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO) (SCHOENOCAULON OFFICINALE SEED - UNII:6NAF1689IO) SCHOENOCAULON OFFICINALE SEED 7 [hp_X] in 1 [hp_X] BLACK MUSTARD SEED (UNII: 8LTY55LQ8D) (BLACK MUSTARD SEED - UNII:8LTY55LQ8D) BLACK MUSTARD SEED 6 [hp_X] in 1 [hp_X] URTICA URENS (UNII: IHN2NQ5OF9) (URTICA URENS - UNII:IHN2NQ5OF9) URTICA URENS 6 [hp_X] in 1 [hp_X] WYETHIA HELENIOIDES ROOT (UNII: J10PD1AQ0N) (WYETHIA HELENIOIDES ROOT - UNII:J10PD1AQ0N) WYETHIA HELENIOIDES ROOT 3 [hp_X] in 1 [hp_X] Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61727-052-30 1 [hp_X] in 1 BOTTLE, SPRAY Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 03/24/2014 Labeler - Homeocare Laboratories (088248828) Registrant - Homeocare Laboratories (088248828) Establishment Name Address ID/FEI Business Operations Homeocare Laboratories 088248828 manufacture(61727-052)