Ultra Zinc Cold Therapy

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
Ultra Zinc Cold Therapy
Generic name
ZINCUM GLUCONICUM
Manufacturer
WALGREEN COMPANY
Product type
HUMAN OTC DRUG
SPL set ID
2106d6f6-4ac4-456e-bc1e-fa9dd9600369
SPL ID
4469cb33-4fe5-a8c8-e063-6294a90a0b87
Version
7
Effective date
2025-11-25
Source export date
2026-09-28
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:20:28
Harmonized routes table
Harmonized routes
ORAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings Ask a doctor before use if you have a sensitivity to zinc or are allergic zinc are taking minocycline, doxycycline, tetracycline or are on Coumadin therapy, zinc treatment may inhibit the absorption of these medicines. Stop Use and ask a doctor If symptoms persist beyond 7 days. If pregnant or breast feeding ask health professional before use. Keep Out of Reach of Children In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.