Instant Hand Sanitizer

Manufacturer
First Step Safety Products Corporation | Zhejiang Enchant Cosmetic Co., Ltd.
Effective date
2020-07-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:20:11

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 68% 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,BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW),AMINOMETHYLPROPANOL,ALOE VERA LEAF,HYALURONATE SODIUM,FRAGRANCE LAVENDER & CHIA F-153480

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1000 ml in 1 bottle NDC: 79195-005-01

1000 ml label1000 ml label1000 ml label01000 ml label01000 ml label11000 ml label1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1037039ethanol 68 % Topical GelPSN1
1037039ethanol 0.68 ML/ML Topical GelSCD1
1037039ethanol 68 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79195-005-012022-01-28C16284748780-1d6a99b39-ab6f-a426-e053-dadaa90af4c279195-005 1000ml FIST STEP BY ENCHANT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79195-005-01Instant Hand Sanitizer1000 mL in 1 BOTTLEGEL10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79195-005INSTANT HAND SANITIZER GEL [FIRST STEP SAFETY PRODUCTS CORPORATION]1Legacy NDC, 1 package rows20200706_a9be67aa-b0ab-5fe7-e053-2a95a90add7a.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79195-00579195-005-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
a9be51a2-b68f-1650-e053-2995a90a150fa9be67aa-b0ab-5fe7-e053-2a95a90add7a2020-07-05WarningsExact identifier
spl id: a9be51a2-b68f-1650-e053-2995a90a150f
spl set id: a9be67aa-b0ab-5fe7-e053-2a95a90add7a

Reported adverse events (FAERS/openFDA)#

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