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Fibromyalgia Relief - 61727-321-21 - (ARNICA MONTANA,LACTIC ACID,STRYCHNOS NUX-VOMICA SEED,POTASSIUM PHOSPHATE, DIBASIC,CUPRIC ARSENITE.)

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Drug Information of Fibromyalgia Relief

Product NDC: 61727-321
Proprietary Name: Fibromyalgia Relief
Non Proprietary Name: ARNICA MONTANA,LACTIC ACID,STRYCHNOS NUX-VOMICA SEED,POTASSIUM PHOSPHATE, DIBASIC,CUPRIC ARSENITE.
Active Ingredient(s): 18; 10; 10; 10; 10; 10    [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g & nbsp;   ARNICA MONTANA,LACTIC ACID,STRYCHNOS NUX-VOMICA SEED,POTASSIUM PHOSPHATE, DIBASIC,CUPRIC ARSENITE.
Administration Route(s): SUBLINGUAL
Dosage Form(s): PELLET
Coding System: National Drug Codes(NDC)

Labeler Information of Fibromyalgia Relief

Product NDC: 61727-321
Labeler Name: Homeocare Laboratories
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20120709

Package Information of Fibromyalgia Relief

Package NDC: 61727-321-21
Package Description: 4 g in 1 TUBE (61727-321-21)

NDC Information of Fibromyalgia Relief

NDC Code 61727-321-21
Proprietary Name Fibromyalgia Relief
Package Description 4 g in 1 TUBE (61727-321-21)
Product NDC 61727-321
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ARNICA MONTANA,LACTIC ACID,STRYCHNOS NUX-VOMICA SEED,POTASSIUM PHOSPHATE, DIBASIC,CUPRIC ARSENITE.
Dosage Form Name PELLET
Route Name SUBLINGUAL
Start Marketing Date 20120709
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Homeocare Laboratories
Substance Name ARNICA MONTANA; CUPRIC ARSENITE; LACTIC ACID; MAGNESIUM PHOSPHATE, TRIBASIC, PENTAHYDRATE; POTASSIUM PHOSPHATE, DIBASIC; STRYCHNOS NUX-VOMICA SEED
Strength Number 18; 10; 10; 10; 10; 10
Strength Unit [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g
Pharmaceutical Classes

Complete Information of Fibromyalgia Relief


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