Sniffly Sprinkles (Native Remedies, LLC)


Welcome to the PulseAid listing for the Sniffly Sprinkles drug offered from Native Remedies, LLC. This pharmaceutical is classified as a HUMAN OTC DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN OTC DRUG drug type category.
LABELER NAME / MANUFACTURER: Native Remedies, LLC
NON-PROPRIETARY NAME: Allium cepa, Ferrum phos, Nat mur, Nuz vom, Pulsatilla
SUBSTANCE NAME: ONION; FERROSOFERRIC PHOSPHATE; SODIUM CHLORIDE; STRYCHNOS NUX-VOMICA SEED; PULSATILLA VULGARIS
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: GRANULE
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2013-01-30
END MARKETING DATE: 0000-00-00


Sniffly Sprinkles HUMAN OTC DRUG Details:

Item DescriptionSniffly Sprinkles from Native Remedies, LLC
LABELER NAME: Native Remedies, LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 6; 8; 6; 30; 6([hp_C]/16mg; [hp_X]/16mg; [hp_X]/16mg; [hp_C]/16mg; [hp_C]/16mg)
START MARKETING DATE: 2013-01-30
END MARKETING DATE: 0000-00-00
PRODUCT ID: 68703-026_5130eca8-a93d-4027-9c6c-a5f9427009e3
PRODUCT NDC: 68703-026
APPLICATION NUMBER:

Other ONION; FERROSOFERRIC PHOSPHATE; SODIUM CHLORIDE; STRYCHNOS NUX-VOMICA SEED; PULSATILLA VULGARIS Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Native Remedies, LLCSniffly Sprinkles