NDC 43251-2281

Natralia Eczema and Psoriasis

Sodium Borate, Graphite, Potassium Sulfate, And Sodium Chloride

Natralia Eczema and Psoriasis is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Lacorium Health Usa Inc.. The primary component is Sodium Borate; Graphite; Potassium Sulfate; Sodium Chloride.

Product ID43251-2281_220eb2b9-79fe-4d3e-a53c-cecdfc5d01e7
NDC43251-2281
Product TypeHuman Otc Drug
Proprietary NameNatralia Eczema and Psoriasis
Generic NameSodium Borate, Graphite, Potassium Sulfate, And Sodium Chloride
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2009-01-03
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameLaCorium Health USA Inc.
Substance NameSODIUM BORATE; GRAPHITE; POTASSIUM SULFATE; SODIUM CHLORIDE
Active Ingredient Strength20 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 43251-2281-1

200 mL in 1 BOTTLE (43251-2281-1)
Marketing Start Date2009-01-03
Marketing End Date2022-08-31
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 43251-2281-1 [43251228101]

Natralia Eczema and Psoriasis GEL
Marketing CategoryUNAPPROVED HOMEOPATHIC
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-01-03

Drug Details

Active Ingredients

IngredientStrength
SODIUM BORATE20 [hp_X]/mL

OpenFDA Data

SPL SET ID:fb7be5dc-3d93-441b-860a-a2caa5cacb70
Manufacturer
UNII

NDC Crossover Matching brand name "Natralia Eczema and Psoriasis" or generic name "Sodium Borate, Graphite, Potassium Sulfate, And Sodium Chloride"

NDCBrand NameGeneric Name
0295-9035Natralia Eczema and PsoriasisSodium Borate (20X HPUS), Graphite (6X HPUS), Potassium Sulfate (3X HPUS), Sodium Chloride (12X HPUS)
43251-2281Natralia Eczema and PsoriasisSodium Borate, Graphite, Potassium Sulfate, and Sodium Chloride
43251-2231Flexitol Naturals Eczema and PsoriasisSodium Borate, Graphite, Potassium Sulfate, and Sodium Chloride
43251-2241natraliaSodium Borate, Graphite, Potassium Sulfate, and Sodium Chloride

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.