nausea relief
- Product NDC
- 37808-501
- 11-digit product format
- 378080501
- Labeler code
- 37808
- Product ID
- 37808-501_f8185acc-bd46-4832-8cc4-9eee48fa58e5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Dextrose (glucose), Levulose (fructose), Phosphoric Acid
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- H E B
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2014-11-04
- Marketing end
- 0000-00-00
- Substance
- DEXTROSE; FRUCTOSE; PHOSPHORIC ACID
- Active strength
- 2 g/5mL; g/5mL; mg/5mL
- 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 |
|---|
| 37808-501-26 | 37808050126 | 1 BOTTLE in 1 CARTON (37808-501-26) > 118 mL in 1 BOTTLE | 1 bottle | 2014-11-04 | 0000-00-00 | No | No | Current |