FDA.reportPublic FDA data

Instant Hand Sanitizer

Manufacturer
Mechanical Servants LLC
Effective date
2017-10-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:11:33

Label at a glance#

ProductInstant Hand Sanitizer HAND SANITIZER BEACH
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

■ place enough product in your palm to thoroughly spread on both hands and rub into the skin 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% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

hand sanitizer to help reduce bacterial on the skin

Warnings

WARNINGS SECTION

Flammable, Keep away from fire & flame. For external use only

When using this product

OTC - WHEN USING SECTION

■ do not in or near the eyes.In case of contact, rinse eyes 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 spread on both hands and rub into the skin until dry ■ children under 6 years of age should be supervised when using this product

Other information

SPL UNCLASSIFIED SECTION

■ store below 106°F (41°C) ■ may discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, propylene glycol, acrylates/c10-30 alkyl acrylate crosspolymer, isopropyl alcohol, aminomethylpropanol, isopropyl myristate, caprylyl glycol, fragrance, tocopheryl acetate

Questions or Comments

OTC - QUESTIONS SECTION

1-844-428-2538

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
29485-3000-22020-09-27C16284748780-1ab0e2407-2dde-f274-e053-dbdaa90a6471Drug Facts
29485-3000-52020-09-27C16284748780-1ab0e2407-2dde-f274-e053-dbdaa90a6471Drug Facts
29485-3000-82020-09-27C16284748780-1ab0e2407-2dde-f274-e053-dbdaa90a6471Drug Facts
29485-3000-22020-09-25C16284748780-1ab0e2407-2dde-f274-e053-dbdaa90a6471Drug Facts
29485-3000-52020-09-25C16284748780-1ab0e2407-2dde-f274-e053-dbdaa90a6471Drug Facts
29485-3000-82020-09-25C16284748780-1ab0e2407-2dde-f274-e053-dbdaa90a6471Drug Facts
29485-3000-22020-07-22C16284748780-1ab0e2407-2dde-f274-e053-dbdaa90a6471Drug Facts
29485-3000-52020-07-22C16284748780-1ab0e2407-2dde-f274-e053-dbdaa90a6471Drug Facts
29485-3000-82020-07-22C16284748780-1ab0e2407-2dde-f274-e053-dbdaa90a6471Drug Facts

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
29485-3000INSTANT HAND SANITIZER HAND SANITIZER BEACH (ALCOHOL) LIQUID [MECHANICAL SERVANTS LLC]1Legacy NDC20171010_5b20e8c1-2f4d-5fa6-e053-2a91aa0aec4e.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
29485-300029485-3000-5, 29485-3000-2, 29485-3000-8

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
PHENOXYETHANOLHIE492ZZ3TIACT
CAPRYLYL GLYCOL00YIU5438UIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
ISOPROPYL ALCOHOLND2M416302IACT
ALCOHOL3K9958V90MACTIB
CARBOMER COPOLYMER TYPE A71DD5V995LIACT

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
5b20e8c1-2f52-5fa6-e053-2a91aa0aec4e5b20e8c1-2f4d-5fa6-e053-2a91aa0aec4e2017-10-09WarningsExact identifier
spl id: 5b20e8c1-2f52-5fa6-e053-2a91aa0aec4e
spl set id: 5b20e8c1-2f4d-5fa6-e053-2a91aa0aec4e

Reported adverse events (FAERS/openFDA)#

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