Benzoin Compound Tincture Professional Pack
- Product NDC
- 0395-4209
- 11-digit product format
- 003954209
- Labeler code
- 0395
- Product ID
- 0395-4209_a8760d26-3891-ddd9-e053-2a95a90a2924
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzoin Resin
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Humco Holding Group, Inc.
- Application
- part356
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 1998-03-25
- Marketing end
- 2020-09-30
- Substance
- BENZOIN RESIN
- Active strength
- 1000 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record