FDA.reportPublic FDA data

Cold-EEZE Cold Remedy

Product NDC
71179-350
11-digit product format
711790350
Labeler code
71179
Product ID
71179-350_514358e2-3cb7-5306-e063-6294a90a59bb
Type
HUMAN OTC DRUG
Nonproprietary name
Zinc Gluconate
Dosage form
TABLET, CHEWABLE
Route
ORAL
Labeler
Vespyr Brands LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2021-07-01
Substance
ZINC GLUCONATE
Active strength
13.3 mg/1
Pharmacologic classes
Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 2 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2025-01-11 03:41 UTC · source 2025-01-10excluded productproduct71179-350UExcluded because listing certification expiredexcluded / ndc_excluded.zip0efc9e666f02…f202fb6c5f17…
2025-01-11 03:41 UTC · source 2025-01-10excluded packagepackage71179-35071179-350-24UExcluded because listing certification expiredexcluded / ndc_excluded.zip0efc9e666f02…f202fb6c5f17…

Additional Listing Data#

Finished product
Yes
Brand name base
Cold-EEZE Cold Remedy
Brand name suffix
UltraMELT Chews
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ZINC GLUCONATE13.3 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
U6WSN5SQ1ZInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
04b6992d-c7c5-56c7-e063-6394a90ae8d0Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71179-350-24Cold-EEZE Cold RemedyUltraMELT Chews12 in 1 BLISTER PACKTABLET, CHEWABLE123
71179-350-24Cold-EEZE Cold RemedyUltraMELT Chews2 in 1 BOXTABLET, CHEWABLE23

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71179-350COLD-EEZE COLD REMEDY ULTRAMELT CHEWS (ZINC GLUCONATE) TABLET, CHEWABLE [VESPYR BRANDS INC]2Current NDC, 2 package rows20250112_04b6992d-c7c5-56c7-e063-6394a90ae8d0.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Cold-EEZE Cold Remedy UltraMELT ChewsZINC GLUCONATEVespyr Brands LLC04b6992d-c7c5-56c7-e063-6394a90ae8d02026-05-01WarningsExact identifier
ndc (product): 71179-350

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71179-350-24711790350242 BLISTER PACK in 1 BOX (71179-350-24) / 12 TABLET, CHEWABLE in 1 BLISTER PACK2 blister pack2021-07-01NoNoCurrent