AgoraFear Relief (Native Remedies, LLC)


Welcome to the PulseAid listing for the AgoraFear Relief 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: Aconitum nap, Calc carb, Nat carb
SUBSTANCE NAME: ACONITUM NAPELLUS; OYSTER SHELL CALCIUM CARBONATE, CRUDE; SODIUM CARBONATE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: OCCLUSIVE DRESSING TECHNIQUE
DOSAGE FORM: TABLET
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2012-09-01
END MARKETING DATE: 0000-00-00


AgoraFear Relief HUMAN OTC DRUG Details:

Item DescriptionAgoraFear Relief from Native Remedies, LLC
LABELER NAME: Native Remedies, LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 30; 30; 30([hp_C]/1; [hp_C]/1; [hp_C]/1)
START MARKETING DATE: 2012-09-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 68703-036_66b26b36-b184-4aea-97a9-588f16b6550c
PRODUCT NDC: 68703-036
APPLICATION NUMBER:

Other ACONITUM NAPELLUS; OYSTER SHELL CALCIUM CARBONATE, CRUDE; SODIUM CARBONATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Native Remedies, LLCAgoraFear Relief