PHUEL
- Product NDC
- 71064-0011
- 11-digit product format
- 710640011
- Labeler code
- 71064
- Product ID
- 71064-0011_c0eb24e5-57ce-79e8-e053-2995a90a375b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- MAGNESIUM SULFATE HEPTAHYDRATE
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Relion Manufacturing
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2018-11-07
- Marketing end
- 0000-00-00
- Substance
- MAGNESIUM SULFATE HEPTAHYDRATE
- Active strength
- 6 [hp_X]/mL
- Pharmacologic classes
- Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA],Osmotic Laxative [EPC],Osmotic Activity [MoA],Inhibition Small Intestine Fluid/Electrolyte Absorption [PE],Increased Large Intestinal Motility [PE],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71064-0011-7 | PHUEL | 210 mL in 1 BOTTLE | SOLUTION | 210 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71064-0011 | PHUEL (MAGNESIUM SULFATE HEPTAHYDRATE) SOLUTION [RELION MANUFACTURING] | 1 | Legacy NDC, 1 package rows | 20210427_c0eb2461-47de-4e0e-e053-2a95a90acf60.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71064-0011-7 | 71064001107 | 210 mL in 1 BOTTLE (71064-0011-7) | 210 ml | 2018-11-07 | 0000-00-00 | No | No | Current |