FDA.reportPublic FDA data

Non Sterile Hand Sanitizer

Manufacturer
HR Pharmaceuticals, Inc.
Effective date
2020-05-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:29:12

Label at a glance#

ProductNon Sterile Hand Sanitizer
Active ingredientALCOHOL
Label structure8 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.

Label contents#

Full prescribing information#

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use:

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

OTC - WHEN USING SECTION

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

Stop use  and ask a doctor

OTC - STOP USE SECTION

if irritation occurs.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swalowed. get medical help or contact a Poison Control Ceter right away

Directions:

DOSAGE & ADMINISTRATION SECTION

  • 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:

SPL UNCLASSIFIED SECTION

  • Store between 15-30C(59-86F).
  • Avoid freezing and excessive heat above 40C(104F).

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Water (Aqua), Glycerin, Carbomer, Aloe Bardadensis Leaf Juice, Sodium Hydroxide

Questions

OTC - QUESTIONS SECTION

Call 877-302-1110

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LableLable

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
69464-00369464-003-30

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
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
ALOE VERA LEAFZY81Z83H0XIACT
SODIUM HYDROXIDE55X04QC32IIACT
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
d7732030-4099-bd4c-e053-2995a90a9ecfa5edeb72-8d49-02b2-e053-2995a90afe052022-02-07WarningsExact identifier
spl set id: a5edeb72-8d49-02b2-e053-2995a90afe05

Reported adverse events (FAERS/openFDA)#

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