K-OK Kiddie Calmer (Native Remedies, LLC)


Welcome to the PulseAid listing for the K-OK Kiddie Calmer 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: Aconitinum, silicea
SUBSTANCE NAME: ACONITUM NAPELLUS; SILICON DIOXIDE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: GRANULE
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2012-08-01
END MARKETING DATE: 0000-00-00


K-OK Kiddie Calmer HUMAN OTC DRUG Details:

Item DescriptionK-OK Kiddie Calmer from Native Remedies, LLC
LABELER NAME: Native Remedies, LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 6; 6([hp_C]/100mg; [hp_C]/100mg)
START MARKETING DATE: 2012-08-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 68703-049_838468cd-25e2-4df4-abc4-ddc572984215
PRODUCT NDC: 68703-049
APPLICATION NUMBER:

Other ACONITUM NAPELLUS; SILICON DIOXIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Native Remedies, LLCK-OK Kiddie Calmer