Vateria indica

The resin from the bark of the tree Vateria indica is therapeutically known in Indian traditional systems of medicine (Ayurveda and Siddha). It is known as Sarja rasa in Ayurveda. It is a complex mixture of several triterpenes, hydrocarbons, ketones, alcohols and acids along with small amounts of sesquiterpenes. Vateria indica resin has been used as a traditional medicine for sore throat, chronic bronchitis, rheumatism, diarrhea, and urinary tract disorders. A preparation of the resin along with tender coconut water is used traditionally for burning micturition, leucorrhea, urethritis, duodenal ulcer and diarrhea. Vateria indica resin is used as astringent, antibacterial, antidiarrheal, emmenagogue. Used for chronic bronchitis, piles, skin eruptions, ringworm, scrofula, tubercular glands, ulcers, wounds, boils, urinary discharges, amenorrhea, gonorrhea and syphilis. The resin is used as an antiseptic and anti-inflammatory ointment. Juice from leaves of Vateria indica is applied to cure burns and orally administered to prevent vomiting.

Affygility Solutions has an occupational exposure limit (OEL) and control band assignment for this active pharmaceutical ingredient (API). This monograph also contains the acceptable daily exposure (ADE) value.

Vateria indica

CAS Registry Number:
Unspecified
Synonym:
Sarja rasa
Cost:
$679 USD

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Why do you need this OEL Fastrac monograph?

OEL Fastrac monographs are a cost-effective and convenient way to meet the requirements for PDEs (ADEs) contained in the EMA Guideline on setting health based exposure limits for use in risk identification in the manufacture of different medicinal products in shared facilities (EMA/CHMP/CVMP/SWP/169430/2012), as well as PIC/S and ANVISA requirements, and to obtain the following information:

  • The numerical OEL and control band assignment needed to determine the level of required engineering controls and personal protective equipment
  • A listing of all cited references utilized in the derivation of the OEL and ADE
  • An expert review and discussion with respect to the critical endpoints of concern, the rationale for the choice of endpoints, and dose that is to be used in the derivation of the ADE (PDE), as required by the EMA's Guideline on setting health-based exposure limits for use in risk identification in the manufacture of different medicinal products in shared facilities

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