Product NDC: | 53799-241 |
Proprietary Name: | Nasal Allergy Relief |
Non Proprietary Name: | Cardiospermum, Galphimia glauca, Luffa operculata, Sabadilla |
Active Ingredient(s): | 6; 6; 6; 6 [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL & nbsp; Cardiospermum, Galphimia glauca, Luffa operculata, Sabadilla |
Administration Route(s): | NASAL |
Dosage Form(s): | SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 53799-241 |
Labeler Name: | Similasan AG |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20100515 |
Package NDC: | 53799-241-20 |
Package Description: | 20 mL in 1 BOTTLE, SPRAY (53799-241-20) |
NDC Code | 53799-241-20 |
Proprietary Name | Nasal Allergy Relief |
Package Description | 20 mL in 1 BOTTLE, SPRAY (53799-241-20) |
Product NDC | 53799-241 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Cardiospermum, Galphimia glauca, Luffa operculata, Sabadilla |
Dosage Form Name | SPRAY |
Route Name | NASAL |
Start Marketing Date | 20100515 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Similasan AG |
Substance Name | CARDIOSPERMUM HALICACABUM FLOWERING TOP; GALPHIMIA GLAUCA FLOWERING TOP; LUFFA OPERCULATA FRUIT; SCHOENOCAULON OFFICINALE SEED |
Strength Number | 6; 6; 6; 6 |
Strength Unit | [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL |
Pharmaceutical Classes |