FDA.reportPublic FDA data

Instant Hand Sanitizer

Manufacturer
First Step Safety Products Corporation | Zhejiang Beta Industry And Trade Co., Ltd.
Effective date
2020-07-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:20:12

Label at a glance#

ProductInstant Hand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Wet hands with product and rub briskly until dry./Direcciones Humedezca las monos con el producto y frotelas energicamnte hasta que se seque.

Storage and handling

Do not store above 100 F.May discolor some fabrics.Harmful to wood finishes and plastics./Mas Informacion No guardar a temperatura superior a 40 C.Padria destenir algunas telas.Perjudicial para acabados de madera y plasticos.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use for handwashing to decrease bacteria on the skin./Uso para el lavado de monos y disminucion de las bacterias en la piel.

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

  • Flammable,keep away from fire or flame.For external use only/Advertencias inflamables,conservese lejos fuego o llama.Para uso extreno solo.
  • When using this product for external use on hands only.In case of contact with eyes,rinse with water/Usando este producto Para uso externo solamente.En caso del contacto on ojas ,aclare con el echar agaua.
  • Stop use and ask a doctor If irritation and redness develops or presists.Inerrumpa el uso y consulte con un medico En caso de desarrollar irritacion y enrojecimiento,o de que estos sintomas persistan.
  • Keep out of the reach of children. In case of accidental ingestion,seek professional assistance or contact a Poison Control Center immediately/Quedese fuera de alance de ninos.En caso de ingestion accidental,buscar ayuda profesional o ponerse en contacto con un Centro de Envenenamiento inmediatamente.

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

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

  • Wet hands with product and rub briskly until dry./Direcciones Humedezca las monos con el producto y frotelas energicamnte hasta que se seque.

Other information

STORAGE AND HANDLING SECTION

  • Do not store above 100 F.May discolor some fabrics.Harmful to wood finishes and plastics./Mas Informacion No guardar a temperatura superior a 40 C.Padria destenir algunas telas.Perjudicial para acabados de madera y plasticos.

Inactive ingredients

INACTIVE INGREDIENT SECTION

WATER,CARBOMER COPOLYMER TYPE A,CARBOMER COPOLYMER TYPE A,CARBOMER COPOLYMER TYPE A,LEMON

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

29 ml in 1 bottle NDC: 79195-010-01

29 ml label29 ml label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79195-010-012022-01-28C16284748780-1d6a99b39-42a2-a426-e053-dadaa90af4c279195-010 29ml FIST STEP BY BETA

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79195-010-01Instant Hand Sanitizer29 mL in 1 BOTTLEGEL291

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79195-010INSTANT HAND SANITIZER GEL [FIRST STEP SAFETY PRODUCTS CORPORATION]1Legacy NDC, 1 package rows20200706_a9c0d210-0aac-6276-e053-2995a90a4db3.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
79195-01079195-010-01

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
CARBOMER COPOLYMER TYPE A71DD5V995LIACT
TROLAMINE9O3K93S3TKIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
LEMON24RS0A988OIACT
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
a9c0d8ab-b872-826d-e053-2995a90aba2aa9c0d210-0aac-6276-e053-2995a90a4db32020-07-06WarningsExact identifier
spl id: a9c0d8ab-b872-826d-e053-2995a90aba2a
spl set id: a9c0d210-0aac-6276-e053-2995a90a4db3

Reported adverse events (FAERS/openFDA)#

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