Overview
Zinc chloride is a solution of ions indicated for use in total parenteral nutrition to maintain zinc levels and prevent deficiency syndromes. Zinc chloride was granted FDA approval before 26 June 1986.
Indication
Zinc chloride injections are indicated for use total parenteral nutrition to maintain zinc serum levels and prevent deficiency syndromes.
Associated Conditions
No associated conditions information available.
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
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No clinical trials found
No clinical trials found for this drug
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
---|---|---|---|---|---|
Bestmade Natural Products | 82969-1038 | ORAL | 6 [hp_X] in 6 [hp_X] | 5/26/2025 | |
Exela Pharma Sciences,LLC | 51754-0102 | INTRAVENOUS | 1 mg in 1 mL | 8/27/2021 | |
Hospira, Inc. | 0409-4090 | INTRAVENOUS | 1 mg in 1 mL | 6/25/2021 | |
BM Private Limited | 85816-1038 | ORAL | 6 [hp_X] in 60 mg | 6/23/2025 |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
---|---|---|---|
No EMA approvals found for this drug. |
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
Nutritrace Concentrate for solution for infusion | SIN14341P | INFUSION, SOLUTION CONCENTRATE | 6.815mg/10ml | 4/22/2013 | |
ADDAVEN CONCENTRATE FOR SOLUTION FOR INFUSION | SIN15302P | INFUSION, SOLUTION CONCENTRATE | 1050 mcg/ml | 7/24/2017 | |
PEDITRACE CONCENTRATE FOR PARENTERAL INFUSION | SIN08899P | INJECTION | 521 mcg/ml | 9/4/1996 |
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
---|---|---|---|---|---|
No NMPA approvals found for this drug. |
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
---|---|---|---|---|---|
No PPB approvals found for this drug. |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
---|---|---|---|---|---|
ZINC CHLORIDE 10.6mg/2mL concentrated injection vial | 22876 | Medicine | A | 10/14/1991 | |
ADDAVEN concentrated injection ampoule | 244493 | Medicine | A | 7/29/2016 | |
LISTERINE TOTAL CARE ANTISEPTIC MOUTHWASH bottle | 178347 | Medicine | A | 12/13/2010 | |
DBL ZINC CHLORIDE INJECTION 5mg Zn/2mL (as zinc chloride 10.6mg/2mL) Injection | 16383 | Medicine | A | 10/8/1991 | |
LISTERINE TARTAR CONTROL ANTISEPTIC MOUTHWASH bottle (reformulation) | 201304 | Medicine | A | 9/25/2012 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
---|---|---|---|---|---|
TRACE ELEMENTS SOLUTION INJ | david bull laboratories (pty) ltd. | 00861979 | Solution - Intravenous | 10.42 MG / 5 ML | 12/31/1991 |
PROSOL ASTRINGENT IRRIGATING MEDICAMENT LIQ | dentsply caulk | 02044269 | Liquid - Dental | .15 % | 12/31/1994 |
DERMAGRAN II MOISTURIZING SPRAY 1MG/ML | canadian medical supply inc. | 02018888 | Liquid - Topical | 1 MG / ML | 12/31/1993 |
DERMAGRAN MOISTURIZING SPRAY | canadian medical supply inc. | 00701726 | Spray - Topical | .15 MG / 30 ML | 12/31/1987 |
ZINCUM MURIATICUM GRANULE (6DH-30DH) | homeocan inc. | 01955055 | Tablet - Oral | 6 DH / TAB | 12/31/1991 |
TRACE ELEMENTS INJECTION USP | 00569046 | Solution - Intravenous | 1.67 MG / ML | 12/31/1983 | |
PERIOSELECT ZINC CHLORIDE SOLUTION 1% | sultan healthcare | 00897612 | Solution - Dental | 1 % | 12/31/1992 |
ORAJEL MOUTH-AID | del pharmaceuticals inc. | 00687502 | Gel - Topical
,
Dental | 1 MG / G | 12/31/1986 |
DERMAGRAN II MOISTURIZING SPRAY-1MG/ML | trans canaderm inc. | 02175061 | Liquid - Topical | 1 MG / ML | 1/1/1996 |
FREEZONE LIQ | whitehall-robins inc. | 01931148 | Liquid - Topical | 1.9 % | 12/31/1993 |
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
---|---|---|---|---|---|
No CIMA AEMPS (Spain) approvals found for this drug. |
Philippines FDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Philippines FDA approvals found for this drug. |
Saudi SFDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Saudi SFDA approvals found for this drug. |
Malaysia NPRA Drug Approvals
Approved Product | Company | Registration Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Malaysia NPRA approvals found for this drug. |
UK EMC Drug Information
Medicine Name | MA Holder | MA Number | Pharmaceutical Form | Active Ingredient | Authorization Date |
---|---|---|---|---|---|
No UK EMC drug information found for this drug. |
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