Coniferyl Alcohol
- Product NDC
- 43742-0185
- 11-digit product format
- 437420185
- Labeler code
- 43742
- Product ID
- 43742-0185_0a5b5d9e-9692-4a7c-b9eb-cdf6cad02613
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Coniferyl Alcohol
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2012-10-29
- Marketing end
- 2021-11-22
- Substance
- CONIFERYL ALCOHOL
- Active strength
- 6 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43742-0185-1 | 43742018501 | 30 mL in 1 BOTTLE, DROPPER (43742-0185-1) | 30 ml | 2012-10-29 | 2021-11-22 | No | No | Current |