Morning Sickness
- Product NDC
- 50845-0100
- 11-digit product format
- 508450100
- Labeler code
- 50845
- Product ID
- 50845-0100_f3158bbf-7ff6-47be-8efe-6d3c9a4fa891
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Symphoricarpus racemosus,
- Dosage form
- SPRAY
- Route
- ORAL
- Labeler
- Liddell Laboratories, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2011-05-24
- Marketing end
- 2024-02-25
- Substance
- SYMPHORICARPOS ALBUS FRUIT
- Active strength
- 30 [hp_C]/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 |
|---|
| 50845-0100-1 | 50845010001 | 30 mL in 1 BOTTLE, SPRAY (50845-0100-1) | 30 ml | 2011-05-24 | 2024-02-25 | No | No | Current |