Thuja
- Product NDC
- 54256-057
- 11-digit product format
- 542560057
- Labeler code
- 54256
- Product ID
- 54256-057_14e9c24e-d175-4000-998d-8d7240caaec4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Thuja occidentalis leafy twig
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- BioResource Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2005-05-01
- Marketing end
- 0000-00-00
- Substance
- THUJA OCCIDENTALIS LEAFY TWIG
- Active strength
- 3 [hp_X]/50mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#