Label: ALLERCETIN- euphrasia officinalis, kali iodatum, sabadilla, sticta pulmonaria, histaminum hydrochloricum, quercetin, succinicum acidum, ambrosia artemisiaefolia tablet, chewable
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Contains inactivated NDC Code(s)
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 March 18, 2019
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS:
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INDICATONS:
For the temporary relief of hay fever and pollen allergic symptoms of sneezing, runny nose, itchy and watery eyes, plugged ears, sinus congestion, and headache.* Allercetin can be taken any time during hay fever season, even before symptoms begin.
*Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
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WARNINGS:
In case of overdose, get medical help or contact a Poison Control Center right away. Do not take this product for headache pain for more than 7 days for adults or 5 days for children. 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. As with any medicine, if you are pregnant, may become pregnant, or breastfeeding, seek the advice of a health care professional before using this product. Keep this and all medicines out of the reach of children.
Tamper Evident: Do not use if foil blister backing is broken. Foil backing is printed with product name and lot number.
- KEEP OUT OF REACH OF CHILDREN:
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DIRECTIONS:
Chew 1 tablet slightly and allow to dissolve in the mouth. Adults take one every 2 to 4 hours until symptoms improve. Then take only as needed to maintain your well-being. Children ages 2 to 12 years, use one-half the adult dosage. For children under the age of 2 years, consult your health care professional.
For Best Results: Keep mouth free of food and strong tastes (such as toothpaste, mouthwash and tobacco) for 15 minutes before and after taking this medicine. These substances may interfere with mucosal absorption.
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INDICATIONS:
For the temporary relief of hay fever and pollen allergic symptoms of sneezing, runny nose, itchy and watery eyes, plugged ears, sinus congestion, and headache.* Allercetin can be taken any time during hay fever season, even before symptoms begin.
*Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
- INACTIVE INGREDIENTS:
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QUESTIONS:
Distributed by:
Source Naturals, Inc. P.O. Box 2118. Santa Cruz, CA. USA 95062. www.sourcenaturals.com
- 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 (UNII: 9W34L2CQ9A) (AMBROSIA ARTEMISIIFOLIA - UNII:9W34L2CQ9A) AMBROSIA ARTEMISIIFOLIA 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)
