FDA.reportPublic FDA data

HAND SANITIZER

Manufacturer
ZHEJIANG RIFESHOW COSMETICS CO.,LTD
Effective date
2020-07-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:22:00

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Put enough product in your palm to cover hands and rub hands together briskly until dry. Children under 6 years of age should be supervised when using. Easy to use at your home,office...or while travelling.

Storage and handling

Store below 110℉(43℃) May discolor certain fabrics.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%±5% v/v. Purpose: Antimicrobial

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria on skin

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash appears and lasts.

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

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears and lasts.

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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Put enough product in your palm to cover hands and rub hands together briskly until dry.

Children under 6 years of age should be supervised when using.

Easy to use at your home,office...or while travelling.

Other information

STORAGE AND HANDLING SECTION

Store below 110℉(43℃)

May discolor certain fabrics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Deionized water,glycerol,Carbomer,triethanolamine

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelpackage label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN2
1305100ethanol 0.75 ML/ML Topical GelSCD2
1305100ethanol 75 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
56084-017-012023-07-28C16284748780-10191ceaa-6eb5-198a-e063-dbdaa90aec3ehand sanitizer
56084-017-022023-07-28C16284748780-10191ceaa-6eb5-198a-e063-dbdaa90aec3ehand sanitizer
56084-017-032023-07-28C16284748780-10191ceaa-6eb5-198a-e063-dbdaa90aec3ehand sanitizer
56084-017-042023-07-28C16284748780-10191ceaa-6eb5-198a-e063-dbdaa90aec3ehand sanitizer
56084-017-052023-07-28C16284748780-10191ceaa-6eb5-198a-e063-dbdaa90aec3ehand sanitizer
56084-017-062023-07-28C16284748780-10191ceaa-6eb5-198a-e063-dbdaa90aec3ehand sanitizer
56084-017-072023-07-28C16284748780-10191ceaa-6eb5-198a-e063-dbdaa90aec3ehand sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
56084-017-01HAND SANITIZER3 mL in 1 BOTTLEGEL32
56084-017-02HAND SANITIZER236 mL in 1 BOTTLEGEL2362
56084-017-03HAND SANITIZER980 mL in 1 BOTTLEGEL9802
56084-017-04HAND SANITIZER2000 mL in 1 BOTTLEGEL20002
56084-017-05HAND SANITIZER3780 mL in 1 BOTTLEGEL37802
56084-017-06HAND SANITIZER5000 mL in 1 BOTTLEGEL50002
56084-017-07HAND SANITIZER3 mL in 1 BAGGEL32

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
56084-017HAND SANITIZER (ALCOHOL) GEL [ZHEJIANG RIFESHOW COSMETICS CO.,LTD]2Legacy NDC, 7 package rows20200721_a8b8d6f6-3ba9-1ec3-e053-2995a90a27d1.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
56084-01756084-017-01, 56084-017-02, 56084-017-03, 56084-017-04, 56084-017-05, 56084-017-06, 56084-017-07

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
5-NORBORNENE-2-METHYLOLACRYLATEYR5K75EW22IACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
TROLAMINE9O3K93S3TKIACT

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
aada3dc7-7724-4a9d-e053-2a95a90ab3f7a8b8d6f6-3ba9-1ec3-e053-2995a90a27d12020-07-20WarningsExact identifier
spl id: aada3dc7-7724-4a9d-e053-2a95a90ab3f7
spl set id: a8b8d6f6-3ba9-1ec3-e053-2995a90a27d1

Reported adverse events (FAERS/openFDA)#

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