natralia - 43251-2241-1 - (Sodium Borate, Graphite, Potassium Sulfate, and Sodium Chloride)

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Drug Information of natralia

Product NDC: 43251-2241
Proprietary Name: natralia
Non Proprietary Name: Sodium Borate, Graphite, Potassium Sulfate, and Sodium Chloride
Active Ingredient(s): 6; 3; 20; 12    [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g & nbsp;   Sodium Borate, Graphite, Potassium Sulfate, and Sodium Chloride
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of natralia

Product NDC: 43251-2241
Labeler Name: LaCorium Health International Pty Ltd
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20090301

Package Information of natralia

Package NDC: 43251-2241-1
Package Description: 1 TUBE in 1 CARTON (43251-2241-1) > 56 g in 1 TUBE

NDC Information of natralia

NDC Code 43251-2241-1
Proprietary Name natralia
Package Description 1 TUBE in 1 CARTON (43251-2241-1) > 56 g in 1 TUBE
Product NDC 43251-2241
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Sodium Borate, Graphite, Potassium Sulfate, and Sodium Chloride
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20090301
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name LaCorium Health International Pty Ltd
Substance Name GRAPHITE; POTASSIUM SULFATE; SODIUM BORATE; SODIUM CHLORIDE
Strength Number 6; 3; 20; 12
Strength Unit [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g
Pharmaceutical Classes

Complete Information of natralia


General Information