FDA.reportPublic FDA data

LORO HAND SANITIZER Anti-Bacterial Gel ETHYL ALCOHOL 70% 30 FL OZ (888mL)

Manufacturer
Sun Hing Foods Inc
Effective date
2020-03-30
Label type
HUMAN OTC DRUG LABEL
Version
14
Source
full-release
Hydrated at
2026-05-31 23:26:27

Label at a glance#

ProductLORO Hand Sanitizer
Active ingredientISOPROPYL ALCOHOL, ALCOHOL
Label structure13 sections

Dosage and administration

Place enough product in your palm to cover hands and rub hands together briskly until dry. Children under 6 years of age should be supervised when using LORO.

Storage and handling

Store below 110 Degree F (43 Degree C) May discolor certain fabrics or surfaces

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) (70%, 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. Isopropyl Alcohol (0.2% v/v).
  3. Glycerol (0.25% v/v).
  4. Acrylite Crosspolymer (0.5% v/v).
  5. Ginger Oil (0.25% v/v)/
  6. Water (29% v/v).

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

Ethyl Alcohol 70% v/v, Isopropyl Alcohol 0.5% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

  • Children under 6 years of age should be supervised when using LORO

OTC - WHEN USING 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 a doctor if irritation or rash appears and lasts.

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 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

  • Place enough product in your palm to cover hands and rub hands together briskly until dry.
  • Children under 6 years of age should be supervised when using LORO.

Other information

STORAGE AND HANDLING SECTION

  • Store below 110 Degree F (43 Degree C)
  • May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Acrylite Crosspolymer, Glycerin, Ginger Oil.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

888mL888mL888 mL NDC: 78185-012-01

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78185-012-012022-01-28C16284748780-1d6a99b39-c80a-a426-e053-dadaa90af4c2LORO HAND SANITIZER Anti-Bacterial Gel ETHYL ALCOHOL 70% 30 FL OZ (888mL)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78185-012-01LORO Hand Sanitizer888 mL in 1 BOTTLEGEL88814

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78185-012LORO HAND SANITIZER (ETHYL ALCOHOL 70%) GEL [SUN HING FOODS INC]14Legacy NDC, 1 package rows20200901_ae3687a4-2d46-46ac-e053-2995a90a32ee.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
78185-01278185-012-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOMER INTERPOLYMER TYPE A (55000 CPS)59TL3WG5COIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302ACTIB
ALCOHOL3K9958V90MACTIB
GINGER OILSAS9Z1SVUKIACT

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
ae3687a4-2d47-46ac-e053-2995a90a32eeae3687a4-2d46-46ac-e053-2995a90a32ee2020-03-30WarningsExact identifier
spl id: ae3687a4-2d47-46ac-e053-2995a90a32ee
spl set id: ae3687a4-2d46-46ac-e053-2995a90a32ee

Reported adverse events (FAERS/openFDA)#

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