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Loma Lux Psoriasis - 57520-0712-3 - (Kali bromatum, Natrum sulphuricum, Niccolum Sulphuricum, Kali sulphuricum, Zincum bromatum,)

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Drug Information of Loma Lux Psoriasis

Product NDC: 57520-0712
Proprietary Name: Loma Lux Psoriasis
Non Proprietary Name: Kali bromatum, Natrum sulphuricum, Niccolum Sulphuricum, Kali sulphuricum, Zincum bromatum,
Active Ingredient(s): 3; 1; 4; 2; 4    [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL & nbsp;   Kali bromatum, Natrum sulphuricum, Niccolum Sulphuricum, Kali sulphuricum, Zincum bromatum,
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Loma Lux Psoriasis

Product NDC: 57520-0712
Labeler Name: Apotheca Company
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20110705

Package Information of Loma Lux Psoriasis

Package NDC: 57520-0712-3
Package Description: 1 CARTON in 1 CARTON (57520-0712-3) > 1 BOTTLE in 1 CARTON (57520-0712-2) > 237 mL in 1 BOTTLE (57520-0712-1)

NDC Information of Loma Lux Psoriasis

NDC Code 57520-0712-3
Proprietary Name Loma Lux Psoriasis
Package Description 1 CARTON in 1 CARTON (57520-0712-3) > 1 BOTTLE in 1 CARTON (57520-0712-2) > 237 mL in 1 BOTTLE (57520-0712-1)
Product NDC 57520-0712
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Kali bromatum, Natrum sulphuricum, Niccolum Sulphuricum, Kali sulphuricum, Zincum bromatum,
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20110705
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Apotheca Company
Substance Name NICKEL SULFATE HEXAHYDRATE; POTASSIUM BROMIDE; POTASSIUM SULFATE; SODIUM BROMIDE; ZINC BROMIDE
Strength Number 3; 1; 4; 2; 4
Strength Unit [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmaceutical Classes

Complete Information of Loma Lux Psoriasis


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