Hush hand sanitizer with aloe vera extract

Manufacturer
Hush Cosmetic Products SRL
Effective date
2021-08-17
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:41:58

Label at a glance#

ProductHush hand sanitizer with aloe vera extract
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

Hand Sanitizer to help reduce bacteria that potentially can cause disease. Recommended for repeated use.

Dosage and administration

Place enough product on hands to cover all surfaces.  Rub hands together until dry. Children under 6 years of age should be supervised when using this product. Other information Store below 110 0 F (43 0 C) May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Acohol, 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease.

Recommended for repeated use.

Warnings

WARNINGS SECTION

Flammable. Keep away from heat or flame.

For external use only.

When using this product do not use in or near the eyes. In case of contact, rinse eyes throughly with water.

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.
  • Children under 6 years of age should be supervised when using this product.

Other information

  • Store below 110 0F (43 0C)
  • May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Vera Extract, Carbomero, Glycerin, Fragance (Parfum), Purified Water (Aqua), Triethanolamine

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

45 mL Label

Label_1Label_1

60 mL Label

Label_2Label_2

120 mL Label

Label_3Label_3

240 mL Label

Label_4Label_4

500 mL label

Label_5Label_5

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN4
581662ethanol 0.7 ML/ML Topical GelSCD4
581662ethanol 70 % Topical GelSY4
581662ethyl alcohol 70 % Topical GelSY4

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78442-001-01Hush hand sanitizer with aloe vera extract45 mL in 1 BOTTLE, PLASTICGEL454
78442-001-02Hush hand sanitizer with aloe vera extract60 mL in 1 BOTTLE, PLASTICGEL604
78442-001-03Hush hand sanitizer with aloe vera extract120 mL in 1 BOTTLE, PLASTICGEL1204
78442-001-04Hush hand sanitizer with aloe vera extract240 mL in 1 BOTTLE, PLASTICGEL2404
78442-001-05Hush hand sanitizer with aloe vera extract500 mL in 1 BOTTLE, PLASTICGEL5004
78442-001-06Hush hand sanitizer with aloe vera extract1000 mL in 1 BOTTLE, PLASTICGEL10004
78442-001-07Hush hand sanitizer with aloe vera extract3780 mL in 1 PACKAGEGEL37804

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78442-001HUSH HAND SANITIZER WITH ALOE VERA EXTRACT (ALCOHOL) GEL [HUSH COSMETIC PRODUCTS SRL]4Legacy NDC, 7 package rows20210820_3a7a7429-ba4e-46c6-a655-212fe8e52bba.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78442-00178442-001-01, 78442-001-02, 78442-001-03, 78442-001-04, 78442-001-05, 78442-001-06, 78442-001-07

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
c9c542cf-0c32-f529-e053-2a95a90a12cc3a7a7429-ba4e-46c6-a655-212fe8e52bba2021-08-17WarningsExact identifier
spl id: c9c542cf-0c32-f529-e053-2a95a90a12cc
spl set id: 3a7a7429-ba4e-46c6-a655-212fe8e52bba

Reported adverse events (FAERS/openFDA)#

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