TrustRX Hand Sanitizer

Manufacturer
Clean Cosmetics, LLC
Effective date
2020-10-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:31:45

Label at a glance#

ProductTrustRX Hand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

Hand Sanitizer to help reduce bacteria on the skin that could cause disease. Recommende for repeated use.

Dosage and administration

Place enough product in your palm to thoroughly cover you hands  Rub hands together briskly until dry.  Children under 6 years of age should be supervised when using this product

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • Hand Sanitizer to help reduce bacteria on the skin that could cause disease.
  • Recommende for repeated use.

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external use only

When using this product

OTC - WHEN USING SECTION

do not use in or near eyes. In case of contact, rinse thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or rash appears and lasts

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product in your palm to thoroughly cover you hands 
  • Rub hands together briskly until dry. 
  • Children under 6 years of age should be supervised when using this product

Other information

SPL UNCLASSIFIED SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Deionized Water, Aloe Barbadensis, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Hyaluronic Acid, Panthenol, Polysorbate 20, Fragrance

Questions or comments?

OTC - QUESTIONS SECTION

call 310-425-3030 Monday to Thursday 9am-5pm

Package Labeling:30ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

Package Labeling:160ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle2Bottle2

Package Labeling:500ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle3Bottle3

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN1
582753ethanol 0.7 ML/ML Topical SolutionSCD1
582753ethanol 70 % Topical SolutionSY1
582753ethyl alcohol 70 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80843-001-012022-01-28C16284748780-1d6a99b39-96e4-a426-e053-dadaa90af4c2TrustRX Hand Sanitizer
80843-001-022022-01-28C16284748780-1d6a99b39-96e4-a426-e053-dadaa90af4c2TrustRX Hand Sanitizer
80843-001-032022-01-28C16284748780-1d6a99b39-96e4-a426-e053-dadaa90af4c2TrustRX Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80843-001-01TrustRX Hand Sanitizer30 mL in 1 BOTTLELIQUID301
80843-001-02TrustRX Hand Sanitizer160 mL in 1 BOTTLELIQUID1601
80843-001-03TrustRX Hand Sanitizer500 mL in 1 BOTTLELIQUID5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80843-001TRUSTRX HAND SANITIZER (ALCOHOL) LIQUID [CLEAN COSMETICS, LLC]1Legacy NDC, 3 package rows20201016_cebde667-b01c-4c58-ac0c-3f3139453e3b.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80843-00180843-001-01, 80843-001-02, 80843-001-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

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
b1b9a622-fbad-0c7c-e053-2a95a90ae0f0cebde667-b01c-4c58-ac0c-3f3139453e3b2020-10-15WarningsExact identifier
spl id: b1b9a622-fbad-0c7c-e053-2a95a90ae0f0
spl set id: cebde667-b01c-4c58-ac0c-3f3139453e3b

Reported adverse events (FAERS/openFDA)#

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