Product NDC: | 43857-0100 |
Proprietary Name: | Pneumoforce |
Non Proprietary Name: | Althaea Officinalis, Natrum Carbonicum Rheum Officinale, Verbascum Thapsus, Zingiber Officinale, Aconitum Napellus |
Active Ingredient(s): | 12; 3; 12; 3; 12; 12; 12; 3; 3; 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL & nbsp; Althaea Officinalis, Natrum Carbonicum Rheum Officinale, Verbascum Thapsus, Zingiber Officinale, Aconitum Napellus |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 43857-0100 |
Labeler Name: | BioActive Nutritional, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20130212 |
Package NDC: | 43857-0100-1 |
Package Description: | 30 mL in 1 BOTTLE, DROPPER (43857-0100-1) |
NDC Code | 43857-0100-1 |
Proprietary Name | Pneumoforce |
Package Description | 30 mL in 1 BOTTLE, DROPPER (43857-0100-1) |
Product NDC | 43857-0100 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Althaea Officinalis, Natrum Carbonicum Rheum Officinale, Verbascum Thapsus, Zingiber Officinale, Aconitum Napellus |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20130212 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | BioActive Nutritional, Inc. |
Substance Name | ACONITUM NAPELLUS; ALTHAEA OFFICINALIS ROOT; DROSERA ROTUNDIFOLIA; GINGER; LOBELIA INFLATA; PHOSPHORUS; POTASSIUM DICHROMATE; RHEUM OFFICINALE ROOT; SODIUM CARBONATE; VERBASCUM THAPSUS |
Strength Number | 12; 3; 12; 3; 12; 12; 12; 3; 3; 3 |
Strength Unit | [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL |
Pharmaceutical Classes |