FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Beauty Manufacturing Solutions Corp.
Effective date
2020-05-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:32:18

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure14 sections

Indications and uses

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

Dosage and administration

Place enough product on hands to cover all surfaces. Run hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

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

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Alcohol 80% v/v.

Purpose: antiseptic.

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand sanitizer.

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only.

Flammable.

Keep away from heat or flame.

Do Not Use

OTC - DO NOT USE SECTION

In children less than 2 months of age.

On open skin wounds.

Stop Use and ask a Doctor

OTC - STOP USE SECTION

If irritation occurs.

These maybe signs of a serious condition.

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough product on hands to cover all surfaces.

Run hands together until dry.

Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

STORAGE AND HANDLING SECTION

Store between 15C - 30C (59F - 86F).

Avoid freezing and excessive heat above 40C (104F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

glycerin, hdrogen peroxide, purified water USP

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Keep out of reach of children.

RECENT MAJOR CHANGES SECTION

If swallowed, get medical help or contact a poison Control Cewnter right away.

When Using this product

OTC - WHEN USING SECTION

Keep out of eyesd, ears and mouth.

In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

If irritation occurs.

These maybe signs of a serious condition.

Principal Display panel (Outside and inside) and back panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

30 ml label30 ml label30 ml Clarks's Botanicals Hand sanitizer spray NDC: 11090-103-01

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11090-10211090-102-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
HYDROGEN PEROXIDEBBX060AN9VIACT

Source Document#

Source XML · Source PDF

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
f047874a-4164-226c-e053-2995a90a3edda4d5e2da-131a-2013-e053-2995a90a56042022-12-20WarningsExact identifier
spl set id: a4d5e2da-131a-2013-e053-2995a90a5604

Reported adverse events (FAERS/openFDA)#

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