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ORAL ASSIST - 50048-015-50 - (ORAL ASSIST)

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Drug Information of ORAL ASSIST

Product NDC: 50048-015
Proprietary Name: ORAL ASSIST
Non Proprietary Name: ORAL ASSIST
Active Ingredient(s): 30; 12; 6; 12; 6; 6    [hp_C]/33.33mg; [hp_C]/33.33mg; [hp_X]/33.33mg; [hp_C]/33.33mg; [hp_C]/33.33mg; [hp_X]/33.33mg & nbsp;   ORAL ASSIST
Administration Route(s): ORAL
Dosage Form(s): TINCTURE
Coding System: National Drug Codes(NDC)

Labeler Information of ORAL ASSIST

Product NDC: 50048-015
Labeler Name: W LAST CC
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20100101

Package Information of ORAL ASSIST

Package NDC: 50048-015-50
Package Description: 100 mg in 1 BOTTLE, GLASS (50048-015-50)

NDC Information of ORAL ASSIST

NDC Code 50048-015-50
Proprietary Name ORAL ASSIST
Package Description 100 mg in 1 BOTTLE, GLASS (50048-015-50)
Product NDC 50048-015
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ORAL ASSIST
Dosage Form Name TINCTURE
Route Name ORAL
Start Marketing Date 20100101
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name W LAST CC
Substance Name BELLADONNA LEAF; CALCIUM SULFIDE; FERROSOFERRIC PHOSPHATE; MERCURIUS SOLUBILIS; SALICYLIC ACID; SILICON DIOXIDE
Strength Number 30; 12; 6; 12; 6; 6
Strength Unit [hp_C]/33.33mg; [hp_C]/33.33mg; [hp_X]/33.33mg; [hp_C]/33.33mg; [hp_C]/33.33mg; [hp_X]/33.33mg
Pharmaceutical Classes

Complete Information of ORAL ASSIST


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