999 Hand Sanitizer

Manufacturer
LER V TRADING INC. | China Resources Sanjiu Medical & Pharmaceutical Co., Ltd.
Effective date
2020-04-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:08:26

Label at a glance#

Product999 Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Hand sanitizer to help reduce bacteria on the skin.

Dosage and administration

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

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75 % v/v. 

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external use only.

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 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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water(Aqua), Glycerin, Carbomer Homopolymer, Trolamine, Fragrance (Parfum).

Other Information

SPL UNCLASSIFIED SECTION

STORE BETWEEN 59-86℉(15-30℃)

AVOID FREEZING AND EXCESSIVE HEAT ABOVE 140℉(40℃)

EXP DATE: SEE ON PACKAGE

Product Labels

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FrontFront

DFDF

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1047755ethanol 75 % Topical SolutionPSN1
1047755ethanol 0.75 ML/ML Topical SolutionSCD1
1047755ethanol 75 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76536-391-602022-01-28C16284748780-1d6a99b39-beff-a426-e053-dadaa90af4c23e86b3de-0af8-4ebf-96e0-967f1be32f79

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76536-391-60999 Hand Sanitizer60 mL in 1 TUBELIQUID601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76536-391999 HAND SANITIZER (ALCOHOL) LIQUID [LER V TRADING INC.]1Legacy NDC, 1 package rows20200429_3e86b3de-0af8-4ebf-96e0-967f1be32f79.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
76536-39176536-391-60

Ingredients#

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

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

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
37cd963b-9d48-4505-a7e4-29b60c4a1b333e86b3de-0af8-4ebf-96e0-967f1be32f792020-04-28WarningsExact identifier
spl id: 37cd963b-9d48-4505-a7e4-29b60c4a1b33
spl set id: 3e86b3de-0af8-4ebf-96e0-967f1be32f79

Reported adverse events (FAERS/openFDA)#

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