Vaginitis
- Product NDC
- 50845-0017
- 11-digit product format
- 508450017
- Labeler code
- 50845
- Product ID
- 50845-0017_4c94bef0-0308-4464-91e7-237cb5435f6c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Baptisia tinctoria, Kreosotum, Mercurius iodatus ruber, Mercurius sulphuratus ruber, Nitricum acidum, Platinum metallicum, Sulphur iodatum, Thymus suis
- Dosage form
- SPRAY
- Route
- ORAL
- Labeler
- Liddell Laboratories, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2011-01-13
- Marketing end
- 2022-07-27
- Substance
- BAPTISIA TINCTORIA ROOT; WOOD CREOSOTE; MERCURIC IODIDE; MERCURIC SULFIDE; NITRIC ACID; PLATINUM; SULFUR IODIDE; SUS SCROFA THYMUS
- Active strength
- 3 [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50845-0017-1 | 50845001701 | 30 mL in 1 BOTTLE, SPRAY (50845-0017-1) | 30 ml | 2011-01-13 | 2022-07-27 | No | No | Current |