FDA.reportPublic FDA data

Secret Plus Hand Sanitizer

Manufacturer
Zhejiang Meizhiyuan Cosmetics Co.,Ltd
Effective date
2022-11-18
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:46:40

Label at a glance#

ProductSecret Plus Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Rub a dime sized drop into hands.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 75% v/v.

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Reduces bacteria and viruses on the hands.

Warnings

WARNINGS SECTION

Flammable: Keep away from open flame and high heat

When using this productkeep out of eyes.

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep of reach of children, if shallowed get medical help or contact Pioson Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Rub a dime sized drop into hands.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Glycerin, Propylene Glycol, Carbomer, Triethanolamine, Fragrance, Aloe Barbadensis (Aloe Vera) Gel, Tocopheryl Acetate (Vitamin E), Lactose, Microcrystalline Cellulose, Sucrose, Zea Mays(Corn) Strach, Ultramarines(C177007), Hydroxypropyl Methyl Celulose, FD&C NO.40, D&C Violet NO.2

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80204-016-012022-03-07C16284748780-1d6a99b39-45e8-a426-e053-dadaa90af4c2325143b1-47fe-4792-956e-883a9e1b24f5
80204-016-012022-01-28C16284748780-1d6a99b39-45e8-a426-e053-dadaa90af4c2325143b1-47fe-4792-956e-883a9e1b24f5

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80204-01680204-016-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
TROLAMINE9O3K93S3TKIACT
ALOE VERA LEAFZY81Z83H0XIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
LACTOSE MONOHYDRATEEWQ57Q8I5XIACT
MICROCRYSTALLINE CELLULOSEOP1R32D61UIACT
SUCROSEC151H8M554IACT
CORN STARCH 3-E-DODECENYL SUCCINIC ANHYDRIDE MODIFIEDQG4MW19XYXIACT
ULTRAMARINE BLUEI39WR998BIIACT
HYPROMELLOSE 2910 (15 MPA.S)36SFW2JZ0WIACT
FD&C RED NO. 40WZB9127XOAIACT
D&C VIOLET NO. 2350KA7O6HKIACT
ALCOHOL3K9958V90MACTIB

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
e9bf0ca7-4fe6-456f-9120-923763bfaffb325143b1-47fe-4792-956e-883a9e1b24f52022-11-18WarningsExact identifier
spl id: e9bf0ca7-4fe6-456f-9120-923763bfaffb
spl set id: 325143b1-47fe-4792-956e-883a9e1b24f5

Reported adverse events (FAERS/openFDA)#

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