FDA.reportPublic FDA data

GZE Ice Water SleepingMask

Manufacturer
Guangdong Aimu Biological Technology Co., Ltd.
Effective date
2024-06-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:01:02

Label at a glance#

ProductGZE Ice Water SleepingMask
Active ingredientGARDEN SNAIL MUCIN
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

GARDEN SNAIL MUCIN

INACTIVE INGREDIENT SECTION

SODIUM POLYACRYLATE (8000 MW)

PEG-9 DIGLYCIDYL ETHERISODIUM HYALURONATE CROSSPOLYMER

HEXANEDIOL

CARBOMER 1342

PANTHENOL

BETAINE

STEARIC ACID

ADENOSINE

XANTHAN GUM

CETEARYL OLIVATE

ARGININE

PHENOXYETHANOL

ALLANTOIN

SORBITAN OLIVATE

CAPRYLICICAPRICILAURIC TRIGLYCERIDE

DIMETHICONE

DOSAGE & ADMINISTRATION SECTION

Take a coin-sized amount and spread it evenly over your face.

OTC - PURPOSE SECTION

This ice water sleeping mask is a natural source of vitality,providing great water retaining energy,increasing skin moisture,and creating a firmer,younger skin.

INDICATIONS & USAGE SECTION

Gently apply a proper amount of the mask to face avoiding eyes and mouth area.Tap gently in order to be absorbed.

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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83566-089GZE ICE WATER SLEEPINGMASK (GARDEN SNAIL MUCIN) CREAM [GUANGDONG AIMU BIOLOGICAL TECHNOLOGY CO., LTD.]2Unmatched20240609_196c31dd-e2b0-f425-e063-6394a90a5395.zip

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83566-08983566-089-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM POLYACRYLATE (8000 MW)285CYO341LIACT
PEG-9 DIGLYCIDYL ETHER/SODIUM HYALURONATE CROSSPOLYMER788QAG3W8AIACT
HEXANEDIOLZIA319275IIACT
CARBOMER 1342809Y72KV36IACT
PANTHENOLWV9CM0O67ZIACT
BETAINE3SCV180C9WIACT
STEARIC ACID4ELV7Z65APIACT
ADENOSINEK72T3FS567IACT
XANTHAN GUMTTV12P4NEEIACT
GARDEN SNAIL MUCINBPB1U0R467ACTIB
CETEARYL OLIVATE58B69Q84JOIACT
ARGININE94ZLA3W45FIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ALLANTOIN344S277G0ZIACT
SORBITAN OLIVATEMDL271E3GRIACT
CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDEFJ1H6M2JG9IACT
DIMETHICONE92RU3N3Y1OIACT

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
39f24f68-534b-9130-e063-6294a90ada6c196c31dd-e2b0-f425-e063-6394a90a53952025-07-15WarningsExact identifier
spl set id: 196c31dd-e2b0-f425-e063-6394a90a5395

Reported adverse events (FAERS/openFDA)#

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