Products Details
Rectified Peppermint Oil
Rectified peppermint oil meets United States Pharmacopeia specifications through double distillation and enhanced purity controls. This pharmaceutical-grade material provides the validated quality, comprehensive documentation, and regulatory alignment req
Product Description
Rectified peppermint oil meets United States Pharmacopeia specifications through double distillation and enhanced purity controls. Additional processing removes impurities and standardizes composition to pharmaceutical standards, creating material suitable for drug formulations and regulated OTC products. This pharmaceutical-grade material provides the validated quality, comprehensive documentation, and regulatory alignment required for medicated products and regulated applications.
Key Features
Pharmacopeial Compliance Assured
Meets United States Pharmacopeia specifications through double distillation, making it suitable for drug formulations and regulated OTC products.
Comprehensive Documentation Package
Includes validated Certificate of Analysis, impurity profiles, heavy metals testing, and chain-of-custody records supporting pharmaceutical quality systems.
Enhanced Purity Through Rectification
Double-distilled processing removes impurities and standardizes composition (44-50% menthol) to pharmaceutical-grade standards.
Regulatory Filing Support
Pharmaceutical GMP processing and validated analytical methods provide documentation required for drug applications and regulatory audits.
Technical Requirements
- Store according to pharmaceutical storage guidelines (controlled conditions)
- Required for products regulated as drugs by health authorities
- Follow pharmaceutical GMP handling and documentation practices
- Maintain complete traceability from receipt through use
- Supplier qualification must include pharmaceutical quality system audit
- Enteric-coated capsules for gastrointestinal delivery
- Medicated lozenges and throat preparations
- Regulated OTC oral analgesic products
- Pharmaceutical syrups and liquid formulations
- Topical pharmaceutical gels with drug claims
- Any formulation requiring pharmacopeial-grade ingredients
- Meets United States Pharmacopeia specifications for pharmaceutical use
- Comprehensive documentation supports regulatory filings and audits
- Validated analytical methods ensure compliance confidence
- Chain-of-custody documentation supports pharmaceutical quality systems
- Pharmaceutical GMP processing eliminates regulatory compliance concerns
- Batch-to-batch reliability critical for drug formulations