Product NDC: | 68703-026 |
Proprietary Name: | Sniffly Sprinkles |
Non Proprietary Name: | Allium cepa, Ferrum phos, Nat mur, Nuz vom, Pulsatilla |
Active Ingredient(s): | 8; 6; 6; 6; 30 [hp_X]/16mg; [hp_C]/16mg; [hp_C]/16mg; [hp_X]/16mg; [hp_C]/16mg & nbsp; Allium cepa, Ferrum phos, Nat mur, Nuz vom, Pulsatilla |
Administration Route(s): | ORAL |
Dosage Form(s): | GRANULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68703-026 |
Labeler Name: | Native Remedies, LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20130130 |
Package NDC: | 68703-026-20 |
Package Description: | 20000 mg in 1 BOTTLE, GLASS (68703-026-20) |
NDC Code | 68703-026-20 |
Proprietary Name | Sniffly Sprinkles |
Package Description | 20000 mg in 1 BOTTLE, GLASS (68703-026-20) |
Product NDC | 68703-026 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Allium cepa, Ferrum phos, Nat mur, Nuz vom, Pulsatilla |
Dosage Form Name | GRANULE |
Route Name | ORAL |
Start Marketing Date | 20130130 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Native Remedies, LLC |
Substance Name | FERROSOFERRIC PHOSPHATE; ONION; PULSATILLA VULGARIS; SODIUM CHLORIDE; STRYCHNOS NUX-VOMICA SEED |
Strength Number | 8; 6; 6; 6; 30 |
Strength Unit | [hp_X]/16mg; [hp_C]/16mg; [hp_C]/16mg; [hp_X]/16mg; [hp_C]/16mg |
Pharmaceutical Classes |