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NDC 43742-2082-01 Electrolyte Plus 3; 6; 6; 8; 8; 6; 3; 3; 3; 6; 9; 8; 3; 9; 6; 3; 8; 6; 6; 9; 3; 8; 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; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL Details
Electrolyte Plus 3; 6; 6; 8; 8; 6; 3; 3; 3; 6; 9; 8; 3; 9; 6; 3; 8; 6; 6; 9; 3; 8; 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; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Electrolyte Plus is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by Deseret Biologicals, Inc.. The primary component is ARGININE; ASCORBIC ACID; CHROMIC OXIDE; COPPER; DIBASIC POTASSIUM PHOSPHATE; FERRIC CHLORIDE HEXAHYDRATE; LEUCINE; LEVOCARNITINE; MAGNESIUM CHLORIDE; MAGNESIUM GLUCONATE; MANGANESE CARBONATE; NICKEL; ORNITHINE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; POTAS.
Product Information
| NDC | 43742-2082 |
|---|---|
| Product ID | 43742-2082_fb3013de-ec20-45b9-bd18-db4799494297 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Electrolyte Plus |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Kali Muriaticum, L-Arginine, L-Carnitine, L-Leucine, L-Ornithine, L-Valine, Magnesia Muriatica, Ascorbicum Acidum, Borax, Chromium Oxydatum, Ferrum Muriaticum, Kali Carbonicum, Magnesium Gluconicum Dihydricum, Natrum Muriaticum, Zincum Gluconicum, Cuprum |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | LIQUID |
| Route | ORAL |
| Active Ingredient Strength | 3; 6; 6; 8; 8; 6; 3; 3; 3; 6; 9; 8; 3; 9; 6; 3; 8; 6; 6; 9; 3; 8; 6 |
| Active Ingredient Units | [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; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL |
| Substance Name | ARGININE; ASCORBIC ACID; CHROMIC OXIDE; COPPER; DIBASIC POTASSIUM PHOSPHATE; FERRIC CHLORIDE HEXAHYDRATE; LEUCINE; LEVOCARNITINE; MAGNESIUM CHLORIDE; MAGNESIUM GLUCONATE; MANGANESE CARBONATE; NICKEL; ORNITHINE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; POTAS |
| Labeler Name | Deseret Biologicals, Inc. |
| Pharmaceutical Class | Allergens [CS], Ascorbic Acid [CS], Blood Coagulation Factor [EPC], Calcium [CS], Calculi Dissolution Agent [EPC], Calculi Dissolution Agent [EPC], Carnitine Analog [EPC], Carnitine [CS], Cations, Divalent [CS], Cell-mediated Immunity [PE], Copper Absorpt |
| DEA Schedule | n/a |
| Marketing Category | UNAPPROVED HOMEOPATHIC |
| Application Number | n/a |
| Listing Certified Through | 2024-12-31 |
Package
NDC 43742-2082-01 (43742208201)
| NDC Package Code | 43742-2082-1 |
|---|---|
| Billing NDC | 43742208201 |
| Package | 120 mL in 1 BOTTLE, DROPPER (43742-2082-1) |
| Marketing Start Date | 2023-10-10 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |