LOVLUV Instant Hand Sanitizer Spray 1.7 FL.OZ. (50 mL)

Manufacturer
Cnt Dream. Co., Ltd
Effective date
2020-04-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:05:04

Label at a glance#

ProductLOVLUV Instant Hand Sanitizer
Active ingredientALCOHOL
Label structure13 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 15-30℃ (59-86°F) Avoid freezing and excessive heat above 40℃ (104°F)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

This is a hand sanitizer manufactured according to the Temporary Policy for Preparation of Certain Alcohol-Based Hand Sanitizer Products During the Public Health Emergency (CoViD-19); Guidance for Industry.

The hand sanitizer is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation) consistent with World Health Organization (WHO) recommendations:

  1. Alcohol (ethanol) (USP or Food Chemical Codex (FCC) grade) (80%, volume/volume (v/v)) in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.
  2. Glycerol (1.45% v/v).
  3. Hydrogen peroxide (0.125% v/v).
  4. Sterile distilled water or boiled cold water.

The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

spray activespray active

Alcohol 80% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

spray purposespray purpose

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

spray usespray use

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

Warnings

WARNINGS SECTION

spray warningsspray warnings

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

Do not use

OTC - DO NOT USE SECTION

spray do not usespray do not use

• In children less than 2 months of age
• On open skin wounds

OTC - WHEN USING SECTION

spray when usingspray when using

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

spray stop usespray stop use

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

spray keep outspray keep out

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

Directions

DOSAGE & ADMINISTRATION SECTION

spray directionsspray directions

• 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

spray otherspray other

Store between 15-30℃ (59-86°F)

Avoid freezing and excessive heat above 40℃ (104°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Spray other informationSpray other information

Water, Glycerin, Fragrance, Sodium Hyaluronate, Aloe Barbadensis Leaf Extract, Camellia Sinensis Leaf Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

spray packagespray package

LOVLUV

INSTANT HAND SANITIZER SPRAY

Non-Sterile Solution

Help Reducing Bacteria

Moisturizing

Non-Sticky

Net 1.7 FL.OZ. (50 mL)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1241663ethanol 80 % Topical SprayPSN1
1241663ethanol 0.8 ML/ML Topical SpraySCD1
1241663ethanol 80 % Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71909-4212-32022-01-28C16284748780-1d6a99b39-eef6-a426-e053-dadaa90af4c2LOVLUV Instant Hand Sanitizer Spray 1.7 FL.OZ. (50 mL)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71909-4212-1LOVLUV Instant Hand Sanitizer50 mL in 1 BOTTLE, SPRAYLIQUID501
71909-4212-2LOVLUV Instant Hand Sanitizer24 in 1 CASELIQUID241
71909-4212-3LOVLUV Instant Hand Sanitizer192 in 1 CASELIQUID1921

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71909-4212LOVLUV INSTANT HAND SANITIZER (ALCOHOL) LIQUID [CNT DREAM. CO., LTD]1Legacy NDC, 3 package rows20200406_a2443fd6-c8c1-1016-e053-2a95a90a7bd4.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71909-421271909-4212-1, 71909-4212-2, 71909-4212-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
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
a24456c7-c355-80d8-e053-2995a90a5ae8a2443fd6-c8c1-1016-e053-2a95a90a7bd42020-04-01WarningsExact identifier
spl id: a24456c7-c355-80d8-e053-2995a90a5ae8
spl set id: a2443fd6-c8c1-1016-e053-2a95a90a7bd4

Reported adverse events (FAERS/openFDA)#

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