Electrolyte Plus
- Product NDC
- 43742-0632
- 11-digit product format
- 437420632
- Labeler code
- 43742
- Product ID
- 43742-0632_b83435e0-239d-44db-9907-81105a775af5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Boron Gluconate, Calcium Gluconate, Chromium Gluconate, Cobalt Gluconate, Copper Gluconate, Ferrous Gluconate, Potassium Gluconate, Magnesium Gluconicum Dihydricum, Manganese Gluconate, Sodium Gluconate, Nickel Gluconate, Selenium Dioxide, Zincum Gluconicum, Kali Phosphoricum, Vanadium Metallicum, Calcarea Phosphorica
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-09-01
- Marketing end
- 2023-07-05
- Substance
- BORON GLUCONATE; CALCIUM GLUCONATE; CHROMIUM GLUCONATE; COBALTOUS GLUCONATE; COPPER GLUCONATE; FERROUS GLUCONATE; POTASSIUM GLUCONATE; MAGNESIUM GLUCONATE; MANGANESE GLUCONATE; SODIUM GLUCONATE; NICKEL GLUCONATE; SELENIUM DIOXIDE; ZINC GLUCONATE; POTASSIUM PHOSPHATE, DIBASIC; VANADIUM; TRIBASIC CALCIUM PHOSPHATE
- Active strength
- 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- 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 |
|---|
| 43742-0632-1 | 43742063201 | 120 mL in 1 BOTTLE, DROPPER (43742-0632-1) | 120 ml | 2015-09-01 | 2023-07-05 | No | No | Current |