Product NDC: | 53799-272 |
Proprietary Name: | Ear Wax Relief |
Non Proprietary Name: | Causticum, Graphites, Lachesis, Lycopodium |
Active Ingredient(s): | 12; 15; 12; 12 [hp_X]/10mL; [hp_X]/10mL; [hp_X]/10mL; [hp_X]/10mL & nbsp; Causticum, Graphites, Lachesis, Lycopodium |
Administration Route(s): | AURICULAR (OTIC) |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 53799-272 |
Labeler Name: | Similasan AG |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20030601 |
Package NDC: | 53799-272-11 |
Package Description: | 10 mL in 1 BOTTLE, DROPPER (53799-272-11) |
NDC Code | 53799-272-11 |
Proprietary Name | Ear Wax Relief |
Package Description | 10 mL in 1 BOTTLE, DROPPER (53799-272-11) |
Product NDC | 53799-272 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Causticum, Graphites, Lachesis, Lycopodium |
Dosage Form Name | SOLUTION |
Route Name | AURICULAR (OTIC) |
Start Marketing Date | 20030601 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Similasan AG |
Substance Name | CAUSTICUM; GRAPHITE; LACHESIS MUTA VENOM; LYCOPODIUM CLAVATUM SPORE |
Strength Number | 12; 15; 12; 12 |
Strength Unit | [hp_X]/10mL; [hp_X]/10mL; [hp_X]/10mL; [hp_X]/10mL |
Pharmaceutical Classes |