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Constipation Relief - 61727-304-21 - (ALUMINUM OXIDE,BRYONIA ALBA ROOT,SODIUM CHLORIDE,GRAPHITE,SILICON DIOXIDE.)

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Drug Information of Constipation Relief

Product NDC: 61727-304
Proprietary Name: Constipation Relief
Non Proprietary Name: ALUMINUM OXIDE,BRYONIA ALBA ROOT,SODIUM CHLORIDE,GRAPHITE,SILICON DIOXIDE.
Active Ingredient(s): 10; 8; 10; 10; 8    [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g & nbsp;   ALUMINUM OXIDE,BRYONIA ALBA ROOT,SODIUM CHLORIDE,GRAPHITE,SILICON DIOXIDE.
Administration Route(s): SUBLINGUAL
Dosage Form(s): PELLET
Coding System: National Drug Codes(NDC)

Labeler Information of Constipation Relief

Product NDC: 61727-304
Labeler Name: Homeocare Laboratories
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20120705

Package Information of Constipation Relief

Package NDC: 61727-304-21
Package Description: 4 g in 1 TUBE (61727-304-21)

NDC Information of Constipation Relief

NDC Code 61727-304-21
Proprietary Name Constipation Relief
Package Description 4 g in 1 TUBE (61727-304-21)
Product NDC 61727-304
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ALUMINUM OXIDE,BRYONIA ALBA ROOT,SODIUM CHLORIDE,GRAPHITE,SILICON DIOXIDE.
Dosage Form Name PELLET
Route Name SUBLINGUAL
Start Marketing Date 20120705
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Homeocare Laboratories
Substance Name ALUMINUM OXIDE; BRYONIA ALBA ROOT; GRAPHITE; SILICON DIOXIDE; SODIUM CHLORIDE
Strength Number 10; 8; 10; 10; 8
Strength Unit [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g
Pharmaceutical Classes

Complete Information of Constipation Relief


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