LANSINOH BABY (Lansinoh Laboratories, Inc.)


Welcome to the PulseAid listing for the LANSINOH BABY drug offered from Lansinoh Laboratories, Inc.. 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: Lansinoh Laboratories, Inc.
NON-PROPRIETARY NAME: DIMETHICONE
SUBSTANCE NAME: DIMETHICONE; LANOLIN; ZINC OXIDE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: OINTMENT
MARKETING CATEGORY NAME: OTC MONOGRAPH FINAL
START MARKETING DATE: 2011-01-01
END MARKETING DATE: 0000-00-00


LANSINOH BABY HUMAN OTC DRUG Details:

Item DescriptionLANSINOH BABY from Lansinoh Laboratories, Inc.
LABELER NAME: Lansinoh Laboratories, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 4.25; 13.17; 4.675(g/85g; g/85g; g/85g)
START MARKETING DATE: 2011-01-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 53997-100_7368031e-8bdc-4e44-bd74-87b28bcd04e3
PRODUCT NDC: 53997-100
APPLICATION NUMBER: part347

Other DIMETHICONE; LANOLIN; ZINC OXIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Lansinoh Laboratories, Inc.LANSINOH BABY