MedPath

Zinc gluconate

Generic Name
Zinc gluconate
Drug Type
Small Molecule
Chemical Formula
C12H22O14Zn
CAS Number
4468-02-4
Unique Ingredient Identifier
U6WSN5SQ1Z

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

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

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.

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