Label: ALLERCETIN- euphrasia officinalis, kali iodatum, sabadilla, sticta pulmonaria, histaminum hydrochloricum, quercetin, succinicum acidum, ambrosia artemisiaefolia tablet, chewable
- NDC Code(s): 64471-196-48
- Packager: Source Naturals, Inc.
- 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 October 31, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS:
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PURPOSE:
*Ambrosia Artemisiaefolia – Relieves hay fever symptoms, Euphrasia Officinalis – Relieves itchy, watery eyes, Histaminum Hydrochloricum – Calms histamine response, Kali Iodatum – Relieves sinus congestion, Quercetin – Calms immune system reactivity, Sabadilla – Relieves sneezing and itchy throat, Sticta Pulmonaria – Relieves nasal and chest congestion, Succinicum Acidum – Relieves nasal and chest congestion
*Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
- USES:
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WARNINGS:
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.
Do not use for headache pain for more than 7 days. If symptoms persist, get worse, or are accompanied by a high fever, or if new symptoms occur, consult a physician, because these could be signs of a serious condition.
Tamper Evident: Do not use if foil blister backing is broken. Foil backing is printed with product name and lot number.
DO NOT USE IF ANY BLISTERS ARE BROKEN OR TORN.
Contains milk
- KEEP OUT OF REACH OF CHILDREN:
- DIRECTIONS:
- INACTIVE INGREDIENTS:
- QUESTIONS:
- PACKAGE LABEL DISPLAY:
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INGREDIENTS AND APPEARANCE
ALLERCETIN
euphrasia officinalis, kali iodatum, sabadilla, sticta pulmonaria, histaminum hydrochloricum, quercetin, succinicum acidum, ambrosia artemisiaefolia tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64471-196 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength EUPHRASIA STRICTA (UNII: C9642I91WL) (EUPHRASIA STRICTA - UNII:C9642I91WL) EUPHRASIA STRICTA 6 [hp_X] in 1 mg POTASSIUM IODIDE (UNII: 1C4QK22F9J) (IODIDE ION - UNII:09G4I6V86Q) POTASSIUM IODIDE 6 [hp_X] in 1 mg SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO) (SCHOENOCAULON OFFICINALE SEED - UNII:6NAF1689IO) SCHOENOCAULON OFFICINALE SEED 6 [hp_X] in 1 mg LOBARIA PULMONARIA (UNII: D1YM0P5Z2T) (LOBARIA PULMONARIA - UNII:D1YM0P5Z2T) LOBARIA PULMONARIA 6 [hp_X] in 1 mg HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U) (HISTAMINE - UNII:820484N8I3) HISTAMINE DIHYDROCHLORIDE 12 [hp_X] in 1 mg QUERCETIN (UNII: 9IKM0I5T1E) (QUERCETIN - UNII:9IKM0I5T1E) QUERCETIN 12 [hp_X] in 1 mg SUCCINIC ACID (UNII: AB6MNQ6J6L) (SUCCINIC ACID - UNII:AB6MNQ6J6L) SUCCINIC ACID 12 [hp_X] in 1 mg AMBROSIA ARTEMISIIFOLIA WHOLE (UNII: 9W34L2CQ9A) (AMBROSIA ARTEMISIIFOLIA - UNII:9W34L2CQ9A) AMBROSIA ARTEMISIIFOLIA WHOLE 30 [hp_X] in 1 mg Inactive Ingredients Ingredient Name Strength LACTOSE (UNII: J2B2A4N98G) MAGNESIUM STEARATE (UNII: 70097M6I30) Product Characteristics Color white Score no score Shape ROUND Size 10mm Flavor Imprint Code H Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:64471-196-48 7200 mg in 1 BLISTER PACK; Type 0: Not a Combination Product 09/05/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/05/2014 Labeler - Source Naturals, Inc. (969024228) Registrant - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture(64471-196) , api manufacture(64471-196) , label(64471-196) , pack(64471-196)