Label: LUNGEX II (ginkgo biloba, colon (suis), lung- suis, pancreas suis, germanium sesquioxide, cuprum metallicum, manganum metallicum, stannum metallicum, alpha-ketoglutaricum acidum, citricum acidum, fumaricum acidum, malic acid, pyruvic acid, succinicum acidum, naphthoquinone, arsenicum metallicum, calcarea carbonica, aconiticum acidum, cis, natrum oxalaceticum, phosphorus liquid
-
Contains inactivated NDC Code(s)
NDC Code(s): 44911-0439-1 - Packager: Energique, 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 2, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
-
ACTIVE INGREDIENTS:
(in each drop): 33.30% Of Natrum Oxalaceticum 12X, 30X. 1.11% Of Alpha-Ketoglutaricum Acidum+ 8X, 12X, 30X; Citricum Acidum 8X, 12X, 30X, Pyruvic Acid 8X, 12X, 30X; Arsenicum Metallicum 12X, Calcarea Carbonica 12X, Cuprum Metallicum 12X, Manganum Metallicum 12X, Stannum Metallicum 12X; Colon (Suis) 12X, 30X, Fumaricum Acidum 12X, 30X, Lung (Suis) 12X, 30X, Malicum Acidum 12X, 30X, Pancreas Suis 12X, 30X, Phosphorus 12X, 30X, Succinicum Acidum 12X, 30X; Aconiticum Acidum, Cis- 30X, Naphthochinonum 30X, 0.01% Of Colon (Suis) 6X, Ginkgo Biloba 6X, Lung (Suis) 6X, Pancreas Suis 6X; Cuprum Metallicum 8X, Fumaricum Acidum 8X, Germanium Sesquioxide 8X, Malicum Acidum 8X, Manganum Metallicum 8X, Stannum Metallicum 8X, Succinicum Acidum 8X; Naphthochinonum 9X, 12X; Aconiticum Acidum, Cis- 12X.
- INDICATIONS:
- WARNINGS:
- KEEP OUT OF REACH OF CHILDREN:
- DIRECTIONS:
- INDICATIONS:
- INACTIVE INGREDIENTS:
- QUESTIONS:
- PACKAGE LABEL DISPLAY:
-
INGREDIENTS AND APPEARANCE
LUNGEX II
ginkgo biloba, colon (suis), lung (suis), pancreas suis, germanium sesquioxide, cuprum metallicum, manganum metallicum, stannum metallicum, alpha-ketoglutaricum acidum, citricum acidum, fumaricum acidum, malic acid, pyruvic acid, succinicum acidum, naphthoquinone, arsenicum metallicum, calcarea carbonica, aconiticum acidum, cis, natrum oxalaceticum, phosphorus liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:44911-0439 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GINKGO (UNII: 19FUJ2C58T) (GINKGO - UNII:19FUJ2C58T) GINKGO 6 [hp_X] in 1 mL SUS SCROFA COLON (UNII: 94J255A0UC) (SUS SCROFA COLON - UNII:94J255A0UC) SUS SCROFA COLON 6 [hp_X] in 1 mL SUS SCROFA LUNG (UNII: 7GL3G1COB3) (SUS SCROFA LUNG - UNII:7GL3G1COB3) SUS SCROFA LUNG 6 [hp_X] in 1 mL SUS SCROFA PANCREAS (UNII: 9Y3J3362RY) (SUS SCROFA PANCREAS - UNII:9Y3J3362RY) SUS SCROFA PANCREAS 6 [hp_X] in 1 mL GERMANIUM SESQUIOXIDE (UNII: 96WE91N25T) (GERMANIUM SESQUIOXIDE - UNII:96WE91N25T) GERMANIUM SESQUIOXIDE 8 [hp_X] in 1 mL COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5) COPPER 8 [hp_X] in 1 mL MANGANESE (UNII: 42Z2K6ZL8P) (MANGANESE - UNII:42Z2K6ZL8P) MANGANESE 8 [hp_X] in 1 mL TIN (UNII: 387GMG9FH5) (TIN - UNII:387GMG9FH5) TIN 8 [hp_X] in 1 mL OXOGLURIC ACID (UNII: 8ID597Z82X) (.ALPHA.-KETOGLUTARIC ACID - UNII:8ID597Z82X) OXOGLURIC ACID 8 [hp_X] in 1 mL CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL) ANHYDROUS CITRIC ACID 8 [hp_X] in 1 mL FUMARIC ACID (UNII: 88XHZ13131) (FUMARIC ACID - UNII:88XHZ13131) FUMARIC ACID 8 [hp_X] in 1 mL MALIC ACID (UNII: 817L1N4CKP) (MALIC ACID - UNII:817L1N4CKP) MALIC ACID 8 [hp_X] in 1 mL PYRUVIC ACID (UNII: 8558G7RUTR) (PYRUVIC ACID - UNII:8558G7RUTR) PYRUVIC ACID 8 [hp_X] in 1 mL SUCCINIC ACID (UNII: AB6MNQ6J6L) (SUCCINIC ACID - UNII:AB6MNQ6J6L) SUCCINIC ACID 8 [hp_X] in 1 mL 1,2-NAPHTHOQUINONE (UNII: 804K62F61Q) (1,2-NAPHTHOQUINONE - UNII:804K62F61Q) 1,2-NAPHTHOQUINONE 9 [hp_X] in 1 mL ARSENIC (UNII: N712M78A8G) (ARSENIC - UNII:N712M78A8G) ARSENIC 12 [hp_X] in 1 mL OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I) OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X] in 1 mL ACONITIC ACID (UNII: 93371T1BXP) (ACONITIC ACID - UNII:93371T1BXP) ACONITIC ACID 12 [hp_X] in 1 mL SODIUM DIETHYL OXALACETATE (UNII: 6CA025Y4FG) (DIETHYL OXALACETATE - UNII:15S56468G7) SODIUM DIETHYL OXALACETATE 12 [hp_X] in 1 mL PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS 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:44911-0439-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 09/08/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/08/2017 Labeler - Energique, Inc. (789886132) Registrant - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture(44911-0439) , api manufacture(44911-0439) , label(44911-0439) , pack(44911-0439)
