FDA.reportPublic FDA data

Universal Instant Hand Sanitizer

Manufacturer
Sichuan Rejoy Essence Biotechnology Co., Ltd
Effective date
2020-04-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:06:58

Label at a glance#

ProductUniversal Instant Hand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

Hand Sanitizer to help reduce bacteria on skin.

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Children under 6 years of age should be supervised when using this product

Storage and handling

Store below 106F(41C) May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Uses

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria on skin.

WARNINGS

WARNINGS SECTION

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

When using this product

OTC - DO NOT USE SECTION

When using this product,do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water Stop use and ask doctor if irritation or rash appears and lasts.

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 occurs. These may be signs of a serious condition.

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

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

When using this product

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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Children under 6 years of age should be supervised when using this product

Other information

STORAGE AND HANDLING SECTION

  • Store below 106F(41C)
  • May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified Water(Aqua), Carbomer, Gluconate Glycerin, Triclosan, Honeysuckle.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

303011841184505054546060887887300300100100500500237237

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN1
1305100ethanol 0.75 ML/ML Topical GelSCD1
1305100ethanol 75 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74034-005-012021-07-23C16284748780-1c7ccaba7-1dc1-fd44-e053-dadaa90aa01ba37d43ca-0d8d-e521-e053-2995a90ab693
74034-005-022021-07-23C16284748780-1c7ccaba7-1dc1-fd44-e053-dadaa90aa01ba37d43ca-0d8d-e521-e053-2995a90ab693
74034-005-032021-07-23C16284748780-1c7ccaba7-1dc1-fd44-e053-dadaa90aa01ba37d43ca-0d8d-e521-e053-2995a90ab693
74034-005-042021-07-23C16284748780-1c7ccaba7-1dc1-fd44-e053-dadaa90aa01ba37d43ca-0d8d-e521-e053-2995a90ab693
74034-005-052021-07-23C16284748780-1c7ccaba7-1dc1-fd44-e053-dadaa90aa01ba37d43ca-0d8d-e521-e053-2995a90ab693
74034-005-062021-07-23C16284748780-1c7ccaba7-1dc1-fd44-e053-dadaa90aa01ba37d43ca-0d8d-e521-e053-2995a90ab693
74034-005-072021-07-23C16284748780-1c7ccaba7-1dc1-fd44-e053-dadaa90aa01ba37d43ca-0d8d-e521-e053-2995a90ab693
74034-005-082021-07-23C16284748780-1c7ccaba7-1dc1-fd44-e053-dadaa90aa01ba37d43ca-0d8d-e521-e053-2995a90ab693
74034-005-092021-07-23C16284748780-1c7ccaba7-1dc1-fd44-e053-dadaa90aa01ba37d43ca-0d8d-e521-e053-2995a90ab693
74034-005-102021-07-23C16284748780-1c7ccaba7-1dc1-fd44-e053-dadaa90aa01ba37d43ca-0d8d-e521-e053-2995a90ab693

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74034-005-01Universal Instant Hand Sanitizer30 mL in 1 BOTTLELIQUID301
74034-005-02Universal Instant Hand Sanitizer50 mL in 1 BOTTLELIQUID501
74034-005-03Universal Instant Hand Sanitizer54 mL in 1 BOTTLELIQUID541
74034-005-04Universal Instant Hand Sanitizer60 mL in 1 BOTTLELIQUID601
74034-005-05Universal Instant Hand Sanitizer100 mL in 1 BOTTLELIQUID1001
74034-005-06Universal Instant Hand Sanitizer237 mL in 1 BOTTLELIQUID2371
74034-005-07Universal Instant Hand Sanitizer300 mL in 1 BOTTLELIQUID3001
74034-005-08Universal Instant Hand Sanitizer500 mL in 1 BOTTLELIQUID5001
74034-005-09Universal Instant Hand Sanitizer887 mL in 1 BOTTLELIQUID8871
74034-005-10Universal Instant Hand Sanitizer1183 mL in 1 BOTTLELIQUID11831

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74034-005UNIVERSAL INSTANT HAND SANITIZER LIQUID [SICHUAN REJOY ESSENCE BIOTECHNOLOGY CO., LTD]1Legacy NDC, 10 package rows20200420_a37d43ca-0d8d-e521-e053-2995a90ab693.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74034-00574034-005-01, 74034-005-03, 74034-005-02, 74034-005-04, 74034-005-05, 74034-005-06, 74034-005-07, 74034-005-08, 74034-005-09, 74034-005-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLUCONATE IONW552L9Y4VZIACT
LONICERA CAPRIFOLIUM FLOWER5N1WD9784UIACT
TRICLOSAN4NM5039Y5XIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER 934Z135WT9208IACT
WATER059QF0KO0RIACT
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
a37c9d9d-52da-23ff-e053-2995a90a8f76a37d43ca-0d8d-e521-e053-2995a90ab6932020-04-17WarningsExact identifier
spl id: a37c9d9d-52da-23ff-e053-2995a90a8f76
spl set id: a37d43ca-0d8d-e521-e053-2995a90ab693

Reported adverse events (FAERS/openFDA)#

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