Label: LUNG DISTRESS (blatta orientalis, bryonia (alba), carbo vegetabilis, eupatorium perfoliatum, histaminum hydrochloricum, iodium, ipecacuanha, lung suis, natrum sulphuricum, nitricum acidum, pulsatilla- pratensis, quebracho, sambucus nigra, sticta pulmonaria, urtica urens spray
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Contains inactivated NDC Code(s)
NDC Code(s): 50845-0275-1, 50845-0275-2 - Packager: Liddell Laboratories
- 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 5, 2021
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ACTIVE INGREDIENTS:
(in each spray) 6.25% of Blatta Orientalis 30C, Bryonia 6X, Carbo Vegetabilis 12X, Eupatorium Perfoliatum 6X, Histaminum Hydrochloricum 200C, Iodium 200C, Ipecacuanha 4X, Lung Suis 6X, Natrum Sulphuricum 30C, Nitricum Acidum 200C, Pulsatilla (Pratensis) 30C, Quebracho 12X, Sambucus Nigra 3X, Sticta Pulmonaria 200C, Urtica Urens 6X, 200C.
- USES:
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WARNINGS:
Do not use if you have ever had an allergic reaction to this product or any of its ingredients.
Stop use and ask a doctor if symptoms persist for more that 3 days, worsen, or if new symptoms occur.
Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away.
If pregnant or breast-feeding, ask a health professional before use.
OTHER INFORMATION: Store at room temperature.
Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.
- KEEP OUT OF REACH OF CHILDREN:
- DIRECTIONS:
- INDICATIONS:
- INACTIVE INGREDIENTS:
- QUESTIONS:
- PACKAGE LABEL DISPLAY:
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INGREDIENTS AND APPEARANCE
LUNG DISTRESS
blatta orientalis, bryonia (alba), carbo vegetabilis, eupatorium perfoliatum, histaminum hydrochloricum, iodium, ipecacuanha, lung suis, natrum sulphuricum, nitricum acidum, pulsatilla (pratensis), quebracho, sambucus nigra, sticta pulmonaria, urtica urens sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50845-0275 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BLATTA ORIENTALIS (UNII: 535787266D) (BLATTA ORIENTALIS - UNII:535787266D) BLATTA ORIENTALIS 30 [hp_C] in 1 mL BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B) BRYONIA ALBA ROOT 6 [hp_X] in 1 mL ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (ACTIVATED CHARCOAL - UNII:2P3VWU3H10) ACTIVATED CHARCOAL 12 [hp_X] in 1 mL EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E) (EUPATORIUM PERFOLIATUM FLOWERING TOP - UNII:1W0775VX6E) EUPATORIUM PERFOLIATUM FLOWERING TOP 6 [hp_X] in 1 mL HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U) (HISTAMINE - UNII:820484N8I3) HISTAMINE DIHYDROCHLORIDE 200 [hp_C] in 1 mL IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE 200 [hp_C] in 1 mL IPECAC (UNII: 62I3C8233L) (IPECAC - UNII:62I3C8233L) IPECAC 4 [hp_X] in 1 mL SUS SCROFA LUNG (UNII: 7GL3G1COB3) (SUS SCROFA LUNG - UNII:7GL3G1COB3) SUS SCROFA LUNG 6 [hp_X] in 1 mL SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM SULFATE ANHYDROUS - UNII:36KCS0R750) SODIUM SULFATE 30 [hp_C] in 1 mL NITRIC ACID (UNII: 411VRN1TV4) (NITRIC ACID - UNII:411VRN1TV4) NITRIC ACID 200 [hp_C] in 1 mL PULSATILLA PRATENSIS WHOLE (UNII: 8E272251DI) (PULSATILLA PRATENSIS WHOLE - UNII:8E272251DI) PULSATILLA PRATENSIS WHOLE 30 [hp_C] in 1 mL ASPIDOSPERMA QUEBRACHO-BLANCO BARK (UNII: 52B1340190) (ASPIDOSPERMA QUEBRACHO-BLANCO BARK - UNII:52B1340190) ASPIDOSPERMA QUEBRACHO-BLANCO BARK 12 [hp_X] in 1 mL SAMBUCUS NIGRA FLOWERING TOP (UNII: CT03BSA18U) (SAMBUCUS NIGRA FLOWERING TOP - UNII:CT03BSA18U) SAMBUCUS NIGRA FLOWERING TOP 3 [hp_X] in 1 mL LOBARIA PULMONARIA (UNII: D1YM0P5Z2T) (LOBARIA PULMONARIA - UNII:D1YM0P5Z2T) LOBARIA PULMONARIA 200 [hp_C] in 1 mL URTICA URENS WHOLE (UNII: IHN2NQ5OF9) (URTICA URENS - UNII:IHN2NQ5OF9) URTICA URENS WHOLE 6 [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:50845-0275-2 1 in 1 CARTON 10/05/2021 1 NDC:50845-0275-1 30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 10/05/2021 Labeler - Liddell Laboratories (832264241) Registrant - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture(50845-0275) , api manufacture(50845-0275) , label(50845-0275) , pack(50845-0275)
