DR WALTONS VAPOR RUB (DR. WALTONS, INCORPORATED)


Welcome to the PulseAid listing for the DR WALTONS VAPOR RUB drug offered from DR. WALTONS, INCORPORATED. 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: DR. WALTONS, INCORPORATED
NON-PROPRIETARY NAME: VAPOR RUB
SUBSTANCE NAME: CAMPHOR (SYNTHETIC); MENTHOL; EUCALYPTUS OIL
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: GEL
MARKETING CATEGORY NAME: OTC MONOGRAPH FINAL
START MARKETING DATE: 2011-07-14
END MARKETING DATE: 0000-00-00


DR WALTONS VAPOR RUB HUMAN OTC DRUG Details:

Item DescriptionDR WALTONS VAPOR RUB from DR. WALTONS, INCORPORATED
LABELER NAME: DR. WALTONS, INCORPORATED
DEA SCHEDULE:
ACTIVE STRENGTH: 5.3; 2.26; 1.13(g/113g; g/113g; g/113g)
START MARKETING DATE: 2011-07-14
END MARKETING DATE: 0000-00-00
PRODUCT ID: 76271-004_84149f61-14f9-44af-b3c3-6dec83130e07
PRODUCT NDC: 76271-004
APPLICATION NUMBER: part346

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