Kreosotum
- Product NDC
- 71919-394
- 11-digit product format
- 719190394
- Labeler code
- 71919
- Product ID
- 71919-394_7e561cc0-aa6f-5462-e053-2991aa0ade77
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- WOOD CREOSOTE
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Washington Homeopathic Products
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2010-02-12
- Marketing end
- 0000-00-00
- Substance
- WOOD CREOSOTE
- Active strength
- 30 [hp_C]/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 71919-394-07 | 71919039407 | 15 mL in 1 VIAL, GLASS (71919-394-07) | 15 ml | 2010-02-12 | 0000-00-00 | No | No | Current |
| 71919-394-08 | 71919039408 | 30 mL in 1 VIAL, GLASS (71919-394-08) | 30 ml | 2010-02-12 | 0000-00-00 | No | No | Current |
| 71919-394-09 | 71919039409 | 50 mL in 1 BOTTLE, GLASS (71919-394-09) | 50 ml | 2010-02-12 | 0000-00-00 | No | No | Current |
| 71919-394-10 | 71919039410 | 100 mL in 1 BOTTLE, GLASS (71919-394-10) | 100 ml | 2010-02-12 | 0000-00-00 | No | No | Current |