NDC Product
Human Otc DrugJust Cbd - Cbd And Thc Ultra Relief NDC 73647-026
- Generic Name
- Menthol, Camphor
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Inactive / Discontinued
This profile provides standardized clinical and technical data for Delta-8-tetrahydrocannabinol, uniquely identified by the FDA Unique Ingredient Identifier (UNII) B49D0HH807.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 5957-75-5 and the RxNorm Concept ID (RxCUI) N/A. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
C21H30O2 HCAWPGARWVBULJ-IAGOWNOFSA-N This section provides a complete list of nomenclature and identifier mappings for Delta-8-tetrahydrocannabinol. Identifiers are organized into official regulatory terms, commercial trade names, and technical systematic synonyms used to ensure accurate identification across clinical pharmaceutical databases, regulatory filings, and electronic health records.
This unique ingredient identifier is listed as an ingredient or substance in the following products in the NDC directory: