FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Yiwu Shining Cosmetics Co., Ltd.
Effective date
2020-05-08
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:10:19

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

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

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

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

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 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.

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.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified Water, Glycerin, Carbomer, Sodium Bicarbonate

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hand Sanitizer 75 BoA Bottle 500mlHand Sanitizer 75 BoA Bottle 500mlHand Sanitizer New Microsoft Bottle 500mlHand Sanitizer New Microsoft Bottle 500mlHand Sanitizer New Bottle 500mlHand Sanitizer New Bottle 500ml

Hand Sanitizer New Bottle 60mlHand Sanitizer New Bottle 60ml

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1047755ethanol 75 % Topical SolutionPSN3
1047755ethanol 0.75 ML/ML Topical SolutionSCD3
1047755ethanol 75 % Topical SolutionSY3

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74862-275-012022-01-28C16284748780-1d6a99b39-d913-a426-e053-dadaa90af4c2a3ffd3b0-1ae2-b268-e053-2a95a90af0eb
74862-275-022022-01-28C16284748780-1d6a99b39-d913-a426-e053-dadaa90af4c2a3ffd3b0-1ae2-b268-e053-2a95a90af0eb
74862-275-032022-01-28C16284748780-1d6a99b39-d913-a426-e053-dadaa90af4c2a3ffd3b0-1ae2-b268-e053-2a95a90af0eb
74862-275-042022-01-28C16284748780-1d6a99b39-d913-a426-e053-dadaa90af4c2a3ffd3b0-1ae2-b268-e053-2a95a90af0eb

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74862-275-01Hand Sanitizer60 mL in 1 BOTTLELIQUID603
74862-275-02Hand Sanitizer500 mL in 1 BOTTLELIQUID5003
74862-275-03Hand Sanitizer500 mL in 1 BOTTLELIQUID5003
74862-275-04Hand Sanitizer500 mL in 1 BOTTLELIQUID5003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74862-275HAND SANITIZER (ALCOHOL) LIQUID [YIWU SHINING COSMETICS CO., LTD.]3Legacy NDC, 4 package rows20200509_a3ffd3b0-1ae2-b268-e053-2a95a90af0eb.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
74862-27574862-275-01, 74862-275-02, 74862-275-03, 74862-275-04

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
SODIUM BICARBONATE8MDF5V39QOIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER 9404Q93RCW27EIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

Source Document#

Source XML · Source PDF

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
a529df44-802f-231c-e053-2995a90a8bb0a3ffd3b0-1ae2-b268-e053-2a95a90af0eb2020-05-08WarningsExact identifier
spl id: a529df44-802f-231c-e053-2995a90a8bb0
spl set id: a3ffd3b0-1ae2-b268-e053-2a95a90af0eb

Reported adverse events (FAERS/openFDA)#

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