FDA.reportPublic FDA data

GZE CUTICLE REMOVER

Manufacturer
Guangzhou Yilong Cosmetics Co., Ltd
Effective date
2024-11-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:36:28

Label at a glance#

ProductGZE CUTICLE REMOVER
Active ingredientCALCIUM GLUCONATE
Label structure10 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Apply around cuticles and under nails.massage nails,wait 10 seconds, push cuticles with manicure stick, wash away excess with warm water.

INACTIVE INGREDIENT SECTION

Aqua

Polyvinyl Acetate

PEG-6 Trimethylolpropane Triacrylate

Lanolin

Phenoxyethanol

Hydrogenated Apricot Kernel Oil

Parfum

OTC - ACTIVE INGREDIENT SECTION

Calcium Gluconate

WARNINGS SECTION

For external use only.

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs.

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin.

OTC - WHEN USING SECTION

When using this product keep out of eyes. Rinse with water to remove.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Apply around cuticles and under nails.massage nails,wait 10 seconds, push cuticles with manicure stick, wash away excess with warm water.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

product imageproduct image

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
CALCIUM CATION Pharmacologic Class Indexing3Indexing - Pharmacologic Class20230427

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
bee4fa8d-8d82-423a-a0b5-40a89dd13a99Product name120250618
e0d2eb29-08bd-4bba-90d1-c91c68a38767Product name420250516
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
334fe8d2-68fb-4331-a576-420e302ec069Product name720240320
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
e92765c1-be81-432a-b909-1b10777ec378Product name120190208
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
0441a8f5-3835-497c-aedd-bc78cba56b2aProduct name120150317
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74458-065-012026-01-29C16284748780-149896155-a7b9-586f-e063-e6dba90add90GZE CUTICLE REMOVER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74458-065-01GZE CUTICLE REMOVER20 mL in 1 BOTTLE, DROPPERLIQUID201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74458-065GZE CUTICLE REMOVER (CALCIUM GLUCONATE 1.5%) LIQUID [GUANGZHOU YILONG COSMETICS CO., LTD]11 package rows20241110_26774793-483b-95bb-e063-6394a90a5d4e.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74458-06574458-065-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
PHENOXYETHANOLHIE492ZZ3TIACT
APRICOT KERNEL OIL PEG-6 ESTERSDRG3KJZ1TJIACT
POLYVINYL ACETATE32K497ZK2UIACT
AQUA059QF0KO0RIACT
TRIMETHYLOLPROPANE TRIACRYLATE4B67KGL96SIACT
CALCIUM GLUCONATESQE6VB453KACTIB
LANOLIN7EV65EAW6HIACT

Source Document#

Source XML

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
26774793-483c-95bb-e063-6394a90a5d4e26774793-483b-95bb-e063-6394a90a5d4e2024-11-09WarningsExact identifier
spl id: 26774793-483c-95bb-e063-6394a90a5d4e
spl set id: 26774793-483b-95bb-e063-6394a90a5d4e

Reported adverse events (FAERS/openFDA)#

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