FDA.reportPublic FDA data

hand sanitizer gel

Manufacturer
ZHEJIANG RIFESHOW COSMETICS CO.,LTD
Effective date
2020-06-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:15:55

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 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

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.

Do not use

OTC - DO NOT USE SECTION

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

OTC - STOP USE SECTION


Stop use and ask a doctor if irritation or rash appear 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 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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
56084-015-012023-07-28C16284748780-10191ceaa-6531-198a-e063-dbdaa90aec3ehand sanitizer gel
56084-015-022023-07-28C16284748780-10191ceaa-6531-198a-e063-dbdaa90aec3ehand sanitizer gel
56084-015-032023-07-28C16284748780-10191ceaa-6531-198a-e063-dbdaa90aec3ehand sanitizer gel
56084-015-042023-07-28C16284748780-10191ceaa-6531-198a-e063-dbdaa90aec3ehand sanitizer gel
56084-015-052023-07-28C16284748780-10191ceaa-6531-198a-e063-dbdaa90aec3ehand sanitizer gel
56084-015-062023-07-28C16284748780-10191ceaa-6531-198a-e063-dbdaa90aec3ehand sanitizer gel
56084-015-072023-07-28C16284748780-10191ceaa-6531-198a-e063-dbdaa90aec3ehand sanitizer gel
56084-015-082023-07-28C16284748780-10191ceaa-6531-198a-e063-dbdaa90aec3ehand sanitizer gel
56084-015-092023-07-28C16284748780-10191ceaa-6531-198a-e063-dbdaa90aec3ehand sanitizer gel
56084-015-102023-07-28C16284748780-10191ceaa-6531-198a-e063-dbdaa90aec3ehand sanitizer gel
56084-015-112023-07-28C16284748780-10191ceaa-6531-198a-e063-dbdaa90aec3ehand sanitizer gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
56084-015-01Hand Sanitizer29 mL in 1 BOTTLEGEL291
56084-015-02Hand Sanitizer60 mL in 1 BOTTLEGEL601
56084-015-03Hand Sanitizer80 mL in 1 BOTTLEGEL801
56084-015-04Hand Sanitizer100 mL in 1 BOTTLEGEL1001
56084-015-05Hand Sanitizer120 mL in 1 BOTTLEGEL1201
56084-015-06Hand Sanitizer250 mL in 1 BOTTLEGEL2501
56084-015-07Hand Sanitizer260 mL in 1 BOTTLEGEL2601
56084-015-08Hand Sanitizer300 mL in 1 BOTTLEGEL3001
56084-015-09Hand Sanitizer473 mL in 1 BOTTLEGEL4731
56084-015-10Hand Sanitizer500 mL in 1 BOTTLEGEL5001
56084-015-11Hand Sanitizer930 mL in 1 BOTTLEGEL9301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
56084-015HAND SANITIZER (ALCOHOL) GEL [ZHEJIANG RIFESHOW COSMETICS CO.,LTD]1Legacy NDC, 11 package rows20200604_a72587ed-66d3-8a6d-e053-2a95a90af5b0.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
56084-01556084-015-01, 56084-015-02, 56084-015-03, 56084-015-04, 56084-015-05, 56084-015-06, 56084-015-07, 56084-015-08, 56084-015-09, 56084-015-10, 56084-015-11

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
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
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
a7256af8-f63a-56a8-e053-2a95a90a7662a72587ed-66d3-8a6d-e053-2a95a90af5b02020-06-02WarningsExact identifier
spl id: a7256af8-f63a-56a8-e053-2a95a90a7662
spl set id: a72587ed-66d3-8a6d-e053-2a95a90af5b0

Reported adverse events (FAERS/openFDA)#

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