Overview
Zinc gluconate is a zinc salt of gluconic acid comprised of two gluconic acid molecules for each zinc cation (2+). Zinc gluconate is a generally recognized as safe (GRAS) substance by FDA . It is available as a trace mineral supplement and over the counter as a lozenge form for a reduced duration of common colds and with decreased symptom severity. Although it has been nasally administered for treating the common cold, this route of administration has been associated with some cases of anosmia , , , . Studies show that zinc may be better absorbed in humans in the gluconate form , , however, results from other studies may vary. Interestingly, zinc supplementation has become a critical intervention for treating diarrheal episodes in children. Studies suggest that administration of zinc along with new low osmolarity oral rehydration solutions/salts (oral rehydration solution), may reduce both the duration and severity of diarrheal episodes for up to 12 weeks . More information about Zinc (in its natural form) is available at Zinc.
Indication
Zinc gluconate is mainly indicated in conditions like zinc deficiency, and can also be administered in adjunctive therapy as an alternative drug of choice in diarrhea .
Associated Conditions
- Zinc Deficiency
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2023/11/07 | Phase 2 | Recruiting | |||
2022/09/06 | Phase 2 | Completed | |||
2021/10/20 | Early Phase 1 | Completed | |||
2019/05/21 | Early Phase 1 | Recruiting | Second Affiliated Hospital, School of Medicine, Zhejiang University | ||
2016/11/01 | Not Applicable | Completed | Chang Gung Memorial Hospital | ||
2013/11/14 | Phase 1 | UNKNOWN | Main Line Health | ||
2008/06/06 | Phase 1 | Completed | All India Institute of Medical Sciences, New Delhi |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
---|---|---|---|---|---|
BonGeo Pharmaceuticals, Inc. | 52796-174 | ORAL | 5 mg in 1 1 | 2/2/2024 | |
H & C Animal Health LLC | 86137-4159 | ORAL | 0.022 g in 1 mL | 4/8/2025 | |
BonGeo Pharmaceuticals, Inc. | 52796-173 | ORAL | 5 mg in 1 1 | 2/1/2024 | |
BonGeo Pharmaceuticals, Inc. | 52796-177 | ORAL | 5 mg in 1 1 | 2/1/2024 | |
Addison Biological Laboratory, Inc. | 86045-9000 | ORAL | 0.022 g in 1 mL | 4/8/2025 | |
Addison Biological Laboratory, Inc. | 86045-9200 | ORAL | .0165 g in 1 mL | 4/8/2025 | |
Sterling-Knight Pharmaceuticals, LLC | 69336-405 | ORAL | 23 mg in 1 1 | 2/22/2021 |
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 |
---|---|---|---|---|---|
ZINC AGUETTANT CONCENTRATE FOR SOLUTION FOR INFUSION 1 MG/ML | SIN16768P | INFUSION, SOLUTION CONCENTRATE | 1mg/mL | 4/25/2023 |
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 |
---|---|---|---|---|---|
JUNYELT CONCENTRATE FOR SOLUTION FOR INFUSION | N/A | N/A | N/A | 2/18/2019 |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
---|---|---|---|---|---|
Men's Multi | 326959 | Medicine | A | 12/2/2019 | |
Herbsense Zinc Vitamin B Plus | 279921 | Medicine | A | 9/5/2016 | |
BLD Bronchus and Lung Detox Bio Complex | 314304 | Medicine | A | 2/18/2019 | |
Zinc Repair Formula | 356881 | Medicine | A | 3/17/2021 | |
IMUNI IMMUNE DEFENCE | 376333 | Medicine | A | 10/14/2021 | |
Nature's Own Mega Magnesium with Vitamin D3 | 366379 | Medicine | A | 5/18/2021 | |
TeenSleep and Stress | 380170 | Medicine | A | 12/3/2021 | |
Pharmacy Health Zinc + Vitamin C | 431020 | Medicine | A | 12/18/2023 | |
Ultimé Men's Prostate Support | 401470 | Medicine | A | 12/21/2022 | |
Women's Multi | 398933 | Medicine | A | 11/7/2022 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
---|---|---|---|---|---|
CHELATED ZINC TAB 25MG | rheingold food international ltd. | 00633712 | Tablet - Oral | 25 MG / TAB | 12/31/1985 |
ZINC TAB 50MG | anabolic laboratories inc. | 00527424 | Tablet - Oral | 50 MG / TAB | 12/31/1981 |
ZINC GLUCONATE TAB 10MG | nutristar health products (1987) inc. | 00471097 | Tablet - Oral | 10 MG / TAB | 12/31/1979 |
ZINC SUPPLEMENT TAB 20MG | hilcoa, division of jeunique international | 00332593 | Tablet - Oral | 20 MG / TAB | 12/31/1975 |
TRACE MIN TAB | nutri-dyn products ltd. | 00563137 | Tablet - Oral | 39 MG | 12/31/1982 |
CALCIUM - MAGNESIUM - ZINC TAB | nutristar health products (1987) inc. | 00825131 | Tablet - Oral | 8 MG / TAB | 12/31/1992 |
ZINC TAB 50MG | nutristar health products (1987) inc. | 00576433 | Tablet - Oral | 50 MG / TAB | 12/31/1983 |
CHELATED ZINC TAB 50MG | nutra research intl ltd. | 00632163 | Tablet - Oral | 50 MG | 12/31/1986 |
LIPALL PLUS TAB | anabolic laboratories inc. | 00492469 | Tablet - Oral | 1.67 MG / TAB | 12/31/1980 |
CALCIUM MAGNESIUM AVEC VITAMINE D ET ZINC | les aliments nutri-source inc. | 00806579 | Tablet - Oral | 10 MG / TAB | 12/31/1991 |
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. |
Help Us Improve
Your feedback helps us provide better drug information and insights.