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Flexitol Naturals Eczema and Psoriasis - 43251-2231-1 - (Sodium Borate, Graphite, Potassium Sulfate, and Sodium Chloride)

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Drug Information of Flexitol Naturals Eczema and Psoriasis

Product NDC: 43251-2231
Proprietary Name: Flexitol Naturals Eczema and Psoriasis
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 Flexitol Naturals Eczema and Psoriasis

Product NDC: 43251-2231
Labeler Name: LaCorium Health International Pty Ltd
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20090103

Package Information of Flexitol Naturals Eczema and Psoriasis

Package NDC: 43251-2231-1
Package Description: 1 TUBE in 1 CARTON (43251-2231-1) > 56 g in 1 TUBE

NDC Information of Flexitol Naturals Eczema and Psoriasis

NDC Code 43251-2231-1
Proprietary Name Flexitol Naturals Eczema and Psoriasis
Package Description 1 TUBE in 1 CARTON (43251-2231-1) > 56 g in 1 TUBE
Product NDC 43251-2231
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 20090103
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 Flexitol Naturals Eczema and Psoriasis


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