Label: EAR RING- allium cepa, argentum nitricum, chenopodium anthelminticum, dulcamara, ginkgo biloba, chininum sulphuricum, cartilago suis, mucosa nasalis suis, asarum canadense, onosmodium virginianum, natrum salicylicum, carbo vegetabilis, carboneum sulphuratum, cyclamen europaeum, gossypium herbaceum, graphites, kreosotum, phosphorus, plumbum metallicum, theridion, zincum metallicum liquid
- NDC Code(s): 43742-2001-1
- Packager: Deseret Biologicals, 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 May 8, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
-
ACTIVE INGREDIENTS:
Allium Cepa 6X, Argentum Nitricum 6X, Chenopodium Anthelminticum 6X, Dulcamara 6X, Ginkgo Biloba 6X, Chininum Sulphuricum 6X, 12X, 30X, 200X, Cartilago Suis 8X, 12X, 30X, 200X, Mucosa Nasalis Suis 8X, 12X, 30X, 200X, Asarum Canadense 9X, Onosmodium Virginianum 10X, Natrum Salicylicum 10X, 12X, 30X, 200X, Carbo Vegetabilis 12X, Carboneum Sulphuratum 12X, Cyclamen Europaeum 12X, Gossypium Herbaceum 12X, Graphites 12X, Kreosotum 12X, Phosphorus 12X, Plumbum Metallicum 12X, Theridion 12X, Zincum Metallicum 12X.
- HOMEOPATHIC INDICATIONS:
- WARNINGS:
- KEEP OUT OF REACH OF CHILDREN:
- DIRECTIONS:
- HOMEOPATHIC INDICATIONS:
- INACTIVE INGREDIENTS:
- QUESTIONS:
- PACKAGE LABEL DISPLAY:
-
INGREDIENTS AND APPEARANCE
EAR RING
allium cepa, argentum nitricum, chenopodium anthelminticum, dulcamara, ginkgo biloba, chininum sulphuricum, cartilago suis, mucosa nasalis suis, asarum canadense, onosmodium virginianum, natrum salicylicum, carbo vegetabilis, carboneum sulphuratum, cyclamen europaeum, gossypium herbaceum, graphites, kreosotum, phosphorus, plumbum metallicum, theridion, zincum metallicum liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43742-2001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ONION (UNII: 492225Q21H) (ONION - UNII:492225Q21H) ONION 6 [hp_X] in 1 mL SILVER NITRATE (UNII: 95IT3W8JZE) (SILVER CATION - UNII:57N7B0K90A) SILVER NITRATE 6 [hp_X] in 1 mL DYSPHANIA AMBROSIOIDES WHOLE (UNII: 4H5RSU087I) (CHENOPODIUM AMBROSIOIDES - UNII:4H5RSU087I) DYSPHANIA AMBROSIOIDES WHOLE 6 [hp_X] in 1 mL SOLANUM DULCAMARA TOP (UNII: KPS1B1162N) (SOLANUM DULCAMARA TOP - UNII:KPS1B1162N) SOLANUM DULCAMARA TOP 6 [hp_X] in 1 mL GINKGO (UNII: 19FUJ2C58T) (GINKGO - UNII:19FUJ2C58T) GINKGO 6 [hp_X] in 1 mL QUININE SULFATE (UNII: KF7Z0E0Q2B) (QUININE - UNII:A7V27PHC7A) QUININE SULFATE 6 [hp_X] in 1 mL SUS SCROFA CARTILAGE (UNII: 73ECW5WG2F) (SUS SCROFA CARTILAGE - UNII:73ECW5WG2F) SUS SCROFA CARTILAGE 8 [hp_X] in 1 mL SUS SCROFA NASAL MUCOSA (UNII: ID3Z1X61WY) (SUS SCROFA NASAL MUCOSA - UNII:ID3Z1X61WY) SUS SCROFA NASAL MUCOSA 8 [hp_X] in 1 mL ASARUM CANADENSE ROOT (UNII: E2O4O7TQYK) (ASARUM CANADENSE ROOT - UNII:E2O4O7TQYK) ASARUM CANADENSE ROOT 9 [hp_X] in 1 mL ONOSMODIUM VIRGINIANUM (UNII: 604NK4250S) (ONOSMODIUM VIRGINIANUM - UNII:604NK4250S) ONOSMODIUM VIRGINIANUM 10 [hp_X] in 1 mL SODIUM SALICYLATE (UNII: WIQ1H85SYP) (SALICYLIC ACID - UNII:O414PZ4LPZ) SODIUM SALICYLATE 10 [hp_X] in 1 mL ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (ACTIVATED CHARCOAL - UNII:2P3VWU3H10) ACTIVATED CHARCOAL 12 [hp_X] in 1 mL CARBON DISULFIDE (UNII: S54S8B99E8) (CARBON DISULFIDE - UNII:S54S8B99E8) CARBON DISULFIDE 12 [hp_X] in 1 mL CYCLAMEN PURPURASCENS TUBER (UNII: G728143D8Q) (CYCLAMEN PURPURASCENS TUBER - UNII:G728143D8Q) CYCLAMEN PURPURASCENS TUBER 12 [hp_X] in 1 mL GOSSYPIUM HERBACEUM ROOT BARK (UNII: VQN1631P4C) (GOSSYPIUM HERBACEUM ROOT BARK - UNII:VQN1631P4C) GOSSYPIUM HERBACEUM ROOT BARK 12 [hp_X] in 1 mL GRAPHITE (UNII: 4QQN74LH4O) (GRAPHITE - UNII:4QQN74LH4O) GRAPHITE 12 [hp_X] in 1 mL WOOD CREOSOTE (UNII: 3JYG22FD73) (WOOD CREOSOTE - UNII:3JYG22FD73) WOOD CREOSOTE 12 [hp_X] in 1 mL PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS 12 [hp_X] in 1 mL LEAD (UNII: 2P299V784P) (LEAD - UNII:2P299V784P) LEAD 12 [hp_X] in 1 mL THERIDION CURASSAVICUM (UNII: 9Z8D3HEM8L) (THERIDION CURASSAVICUM - UNII:9Z8D3HEM8L) THERIDION CURASSAVICUM 12 [hp_X] in 1 mL ZINC (UNII: J41CSQ7QDS) (ZINC - UNII:J41CSQ7QDS) ZINC 12 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:43742-2001-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 12/21/2020 12/01/2028 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 12/21/2020 12/01/2028 Labeler - Deseret Biologicals, Inc. (940741853) Registrant - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture(43742-2001) , api manufacture(43742-2001) , label(43742-2001) , pack(43742-2001)