Leader Nausea Relief
- Product NDC
- 49781-132
- 11-digit product format
- 497810132
- Labeler code
- 49781
- Product ID
- 49781-132_8b038f91-aa93-458f-bc04-0ed1ed834604
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Dextrose (glucose), Levulose (fructose), Phosphoric Acid
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Cardinal Health
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2015-07-09
- Marketing end
- 2021-10-31
- Substance
- DEXTROSE; FRUCTOSE; PHOSPHORIC ACID
- Active strength
- 2 g/5mL; g/5mL; mg/5mL
- 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 |
|---|
| 49781-132-04 | 49781013204 | 1 BOTTLE in 1 CARTON (49781-132-04) > 118 mL in 1 BOTTLE | 1 bottle | 2015-07-09 | 2021-10-31 | No | No | Current |