TECHNIblock ULTRA SUNSCREEN (The Myles Group LLC)


Welcome to the PulseAid listing for the TECHNIblock ULTRA SUNSCREEN drug offered from The Myles Group 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: The Myles Group LLC
NON-PROPRIETARY NAME: AVOBENZONE,OCTINOXATE,OXYBENZONE,PADIMATE
SUBSTANCE NAME: AVOBENZONE; OCTINOXATE; OXYBENZONE; PADIMATE A
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: LOTION
MARKETING CATEGORY NAME: OTC MONOGRAPH FINAL
START MARKETING DATE: 2010-04-05
END MARKETING DATE: 0000-00-00


TECHNIblock ULTRA SUNSCREEN HUMAN OTC DRUG Details:

Item DescriptionTECHNIblock ULTRA SUNSCREEN from The Myles Group LLC
LABELER NAME: The Myles Group LLC
DEA SCHEDULE:
ACTIVE STRENGTH: .6; 6.3; 3.4; 5.1(mL/100mL; mL/100mL; mL/100mL; mL/100mL)
START MARKETING DATE: 2010-04-05
END MARKETING DATE: 0000-00-00
PRODUCT ID: 49672-100_f2f97861-043b-456a-89d1-505acc6246d1
PRODUCT NDC: 49672-100
APPLICATION NUMBER: part352

Other AVOBENZONE; OCTINOXATE; OXYBENZONE; PADIMATE A Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
The Myles Group LLCTECHNIblock ULTRA SUNSCREEN