FDA.reportPublic FDA data

secret plus Hand Sanitizer

Manufacturer
Zhejiang Meizhiyuan Cosmetics Co., Ltd
Effective date
2020-07-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:21:36

Label at a glance#

Productsecret plus Hand Sanitizer 01
Active ingredientALCOHOL
Label structure11 sections

Label contents#

Full prescribing information#

Drug facts

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Purpose

Ethyl Alcohol 75% v/v ....Antimicrobial

USE

OTC - PURPOSE SECTION

Reduce bacteria and viruses on the hands.

Flammable:

WARNINGS SECTION

Keep away form open flame and high heat.

WHEN USING THIS PRODUCT

OTC - WHEN USING SECTION

Keep out of eyes.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed get immediate medical help or contact a poison control center right away.

Direction:

DOSAGE & ADMINISTRATION SECTION

Rub a dime sized drop into hands.

INDICATIONS & USAGE SECTION

Rub hands together until dry.

Other information

OTHER SAFETY INFORMATION

Store below 110 oF (43 oC).

May discolot certain fabrics or surfaces.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water( aqua), Glycerin, Propylene Glycol, Carbomer, Aminomethyl Propanol, Fragrance, Aloe Barbadensis( Aloe Vera) Gel, Tocopheryl acetate( vitamin E), Lactose, Microcrystalline cellulose, Sucrose, Zea Mays( corn) Starch, Ultramarines( CI77007), Hydroxypropyl Methyl Celulose, FD&C RED No. 40, D&C VIOLET No. 2.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

54304-082-0154304-082-01

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
54304-08254304-082-01

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
SUCROSEC151H8M554IACT
ULTRAMARINE BLUEI39WR998BIIACT
HYPROMELLOSE, UNSPECIFIED3NXW29V3WOIACT
FD&C RED NO. 40WZB9127XOAIACT
CARBOMER 9404Q93RCW27EIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
AMINOMETHYLPROPANOLLU49E6626QIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALCOHOL3K9958V90MACTIB
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
STRAWBERRY4J2TY8Y81VIACT
LACTOSE, UNSPECIFIED FORMJ2B2A4N98GIACT
D&C VIOLET NO. 2350KA7O6HKIACT
STARCH, CORNO8232NY3SJIACT
MICROCRYSTALLINE CELLULOSEOP1R32D61UIACT

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
aa8832c6-207a-6bb4-e053-2995a90aa216a987d951-de39-8b3f-e053-2a95a90a0fd52020-07-16WarningsExact identifier
spl set id: a987d951-de39-8b3f-e053-2a95a90a0fd5

Reported adverse events (FAERS/openFDA)#

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