N-Con Tonic (Native Remedies, LLC)


Welcome to the PulseAid listing for the N-Con Tonic 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: Calc fluor, Equisetum arv, Nat phos, Nat sulphuricum, Pulsatilla, Acacia gum, lactose, magnesium stearate, corn starch, sucrose
SUBSTANCE NAME: CALCIUM FLUORIDE; EQUISETUM ARVENSE TOP; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM SULFATE; PULSATILLA VULGARIS
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: TABLET
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2013-01-16
END MARKETING DATE: 0000-00-00


N-Con Tonic HUMAN OTC DRUG Details:

Item DescriptionN-Con Tonic from Native Remedies, LLC
LABELER NAME: Native Remedies, LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 6; 3; 6; 6; 3([hp_C]/1; [hp_X]/1; [hp_C]/1; [hp_C]/1; [hp_X]/1)
START MARKETING DATE: 2013-01-16
END MARKETING DATE: 0000-00-00
PRODUCT ID: 68703-053_166cc43d-5c7d-4da8-9ca0-6dab8598881d
PRODUCT NDC: 68703-053
APPLICATION NUMBER:

Other CALCIUM FLUORIDE; EQUISETUM ARVENSE TOP; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM SULFATE; PULSATILLA VULGARIS Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Native Remedies, LLCN-Con Tonic