Label: RHINALLERGY- solidago virgaurea flowering top, histamine dihydrochloride, ambrosia artemisiifolia, onion, euphrasia stricta, schoenocaulon officinale seed tablet
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Contains inactivated NDC Code(s)
NDC Code(s): 0220-9315-04 - Packager: Boiron
- 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 February 25, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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PURPOSE
Allium cepa 5C HPUS....relieves runny nose associated with allergies
Ambrosia artemisiaefolia 5C HPUS ...relieves spasmodic cough associated with hay fever
Euphrasia officinalis 5C HPUS ...relieves burning, irritated eyes
Histaminum hydrochloricum 9C HPUS ...relieves symptoms of allergic conditions
Sabadilla 5C HPUS ...relieves sneezing and itchy throat associated with allergies
Solidago virgaurea 5C HPUS ...relieves abundant nasal discharge
- INDICATIONS & USAGE
- INACTIVE INGREDIENT
- HOW SUPPLIED
- STORAGE AND HANDLING
- QUESTIONS
- WARNINGS
- ASK DOCTOR
- STOP USE
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
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DOSAGE & ADMINISTRATION
Adults and children 2 years of age and older: at the onset of symptoms, dissolve 2 tablets under the tongue every 15 minutes for 1 hour, then, dissolve 2 tablets under the tongue 3 times a day until symptoms are relieved.
Children 2 to 6 years of age: Dissolve 2 tablets in 1 tablespoon of water for easier intake. Follow directions above.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
RHINALLERGY
solidago virgaurea flowering top, histamine dihydrochloride, ambrosia artemisiifolia, onion, euphrasia stricta, schoenocaulon officinale seed tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0220-9315 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMBROSIA ARTEMISIIFOLIA (UNII: 9W34L2CQ9A) (AMBROSIA ARTEMISIIFOLIA - UNII:9W34L2CQ9A) AMBROSIA ARTEMISIIFOLIA 5 [hp_C] SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO) (SCHOENOCAULON OFFICINALE SEED - UNII:6NAF1689IO) SCHOENOCAULON OFFICINALE SEED 5 [hp_C] EUPHRASIA STRICTA (UNII: C9642I91WL) (EUPHRASIA STRICTA - UNII:C9642I91WL) EUPHRASIA STRICTA 5 [hp_C] ONION (UNII: 492225Q21H) (ONION - UNII:492225Q21H) ONION 5 [hp_C] SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50) (SOLIDAGO VIRGAUREA FLOWERING TOP - UNII:5405K23S50) SOLIDAGO VIRGAUREA FLOWERING TOP 5 [hp_C] HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U) (HISTAMINE - UNII:820484N8I3) HISTAMINE DIHYDROCHLORIDE 9 [hp_C] Inactive Ingredients Ingredient Name Strength LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) MAGNESIUM STEARATE (UNII: 70097M6I30) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) Product Characteristics Color white Score no score Shape ROUND Size 9mm Flavor Imprint Code BOIRON Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0220-9315-04 60 in 1 BLISTER PACK; Type 0: Not a Combination Product 07/01/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/01/2018 Labeler - Boiron (282560473) Registrant - Boiron, Inc. (014892269) Establishment Name Address ID/FEI Business Operations Boiron 282560473 manufacture(0220-9315)
