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 21:47:15

Label at a glance#

ProductSecret Plus Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

Wet hands thoroughly with product and rub into skin until dry. Children 6 years and younger need adult supervision when using this product.

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F) Store at a temperature not exceeding 30 C. Keep tightly closed Precaution If taken internally, consult a physician. Keep out of reach of children. FLAMMABLE: Keep away from open flame.

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 that may cause disease.

Warnings

WARNINGS SECTION

Flammable: Keep away from open flame.

FOR EXTERNAL USE ONLY.

WHEN USING THIS PRODUCT: Avoid contact with eyes and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.
Stop use and ask a doctor if Irritation or redness develops.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly with product and rub into skin until dry.
  • Children 6 years and younger need adult supervision when using this product.

Other information

STORAGE AND HANDLING SECTION

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)

Store at a temperature not exceeding 30 C.
Keep tightly closed

Precaution

  • If taken internally, consult a physician. Keep out of reach of children.
  • FLAMMABLE: Keep away from open flame.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Glycerin, Propylene Glycol, Carbomer, Aminomethyl propanol, Fragrance, Aloe Barbadensis (Aloe Vera) Gel, Tocopheryl Acetate (Vitamin E).

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80204-012-012022-03-07C16284748780-1d6a99b39-fab6-a426-e053-dadaa90af4c2f5071e6d-a39d-4911-b1be-b3f3059e40dd
80204-012-022022-03-07C16284748780-1d6a99b39-fab6-a426-e053-dadaa90af4c2f5071e6d-a39d-4911-b1be-b3f3059e40dd
80204-012-012022-01-28C16284748780-1d6a99b39-fab6-a426-e053-dadaa90af4c2f5071e6d-a39d-4911-b1be-b3f3059e40dd
80204-012-022022-01-28C16284748780-1d6a99b39-fab6-a426-e053-dadaa90af4c2f5071e6d-a39d-4911-b1be-b3f3059e40dd

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80204-01280204-012-01, 80204-012-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
ALOE VERA LEAFZY81Z83H0XIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
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
838cc605-0b46-4a10-8fb2-14847c7a7ec2f5071e6d-a39d-4911-b1be-b3f3059e40dd2022-11-18WarningsExact identifier
spl id: 838cc605-0b46-4a10-8fb2-14847c7a7ec2
spl set id: f5071e6d-a39d-4911-b1be-b3f3059e40dd

Reported adverse events (FAERS/openFDA)#

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