FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
InMind NutraScience Inc. | GUANGZHOU ORCHARD AROMATHERAPY & SKIN CARE CO.,LTD
Effective date
2020-07-31
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:28:45

Label at a glance#

ProductSaniSMART Hand Sanitizer
Active ingredientALCOHOL
Label structure12 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.

Storage and handling

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

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

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

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

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

  • 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

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Glycerin, Triethanolamine, Water, Polyacrylic acid, Aloe barbadensis leaf extract.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

60 mL NDC: 75721-001-00 LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN2
1305100ethanol 0.75 ML/ML Topical GelSCD2
1305100ethanol 75 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75721-001-002022-01-28C16284748780-1d6a99b39-e256-a426-e053-dadaa90af4c2a2408ce7-082c-e798-e053-2a95a90ae0f5
75721-001-012022-01-28C16284748780-1d6a99b39-e256-a426-e053-dadaa90af4c2a2408ce7-082c-e798-e053-2a95a90ae0f5
75721-001-022022-01-28C16284748780-1d6a99b39-e256-a426-e053-dadaa90af4c2a2408ce7-082c-e798-e053-2a95a90ae0f5
75721-001-032022-01-28C16284748780-1d6a99b39-e256-a426-e053-dadaa90af4c2a2408ce7-082c-e798-e053-2a95a90ae0f5
75721-001-042022-01-28C16284748780-1d6a99b39-e256-a426-e053-dadaa90af4c2a2408ce7-082c-e798-e053-2a95a90ae0f5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75721-001-00SaniSMART Hand Sanitizer60 mL in 1 BOTTLEGEL602
75721-001-01SaniSMART Hand Sanitizer120 mL in 1 BOTTLEGEL1202
75721-001-02SaniSMART Hand Sanitizer250 mL in 1 BOTTLEGEL2502
75721-001-03SaniSMART Hand Sanitizer500 mL in 1 BOTTLEGEL5002
75721-001-04SaniSMART Hand Sanitizer1000 mL in 1 BOTTLEGEL10002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75721-001SANISMART HAND SANITIZER (ALCOHOL) GEL [INMIND NUTRASCIENCE INC.]2Legacy NDC, 5 package rows20200909_a2408ce7-082c-e798-e053-2a95a90ae0f5.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
75721-00175721-001-00, 75721-001-01, 75721-001-02, 75721-001-03, 75721-001-04

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 A (ALLYL PENTAERYTHRITOL CROSSLINKED)71DD5V995LIACT
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
EDETOLQ4R969U9FRIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
abc22d60-0568-79b1-e053-2a95a90ad81ca2408ce7-082c-e798-e053-2a95a90ae0f52020-07-31WarningsExact identifier
spl id: abc22d60-0568-79b1-e053-2a95a90ad81c
spl set id: a2408ce7-082c-e798-e053-2a95a90ae0f5

Reported adverse events (FAERS/openFDA)#

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