M MARVEL SANI CARE Instant Hand Sanitizer

Manufacturer
GUANGZHOU TECHIN DEVELOPMENT CO., LTD
Effective date
2022-03-03
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:48:36

Label at a glance#

ProductM MARVEL SANI CARE Instant Hand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Put proper amount onto palms and rub hands briskly until dry. No washing or rinsing required. Air dries quickly

Storage and handling

Keep in closed container in a cool dry place of ambient temperature between 5-30C (59-86F) Batch and MFG date printed on bottle Validity: 24 mounths from MFG date Made in China

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For daily hand sanitizing, to reduce bateria on hands

Warnings

WARNINGS SECTION

For external use only

Flammable. Keep away from fires and high temperature

OTC - WHEN USING SECTION

Do not use on open skin wounds

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

OTC - STOP USE SECTION

Stop use if irritation or rash occurs, if condition persists, contact a healthcare proactitioner

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

  • Put proper amount onto palms and rub hands briskly until dry.
  • No washing or rinsing required. Air dries quickly

Other information

STORAGE AND HANDLING SECTION

Keep in closed container in a cool dry place of ambient temperature between 5-30C (59-86F)

Batch and MFG date printed on bottle

Validity: 24 mounths from MFG date

Made in China

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Aminomethyl propanol, aloe vera extract, glycerin, carbomer, D-Panthenol, vitamin E

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80107-001-012023-07-28C16284748780-1d6a99b39-c87b-a426-e053-dadaa90af4c2aa5f8929-2e8e-4d19-8b0c-75eed2ff3ddf
80107-001-022023-07-28C16284748780-1d6a99b39-c87b-a426-e053-dadaa90af4c2aa5f8929-2e8e-4d19-8b0c-75eed2ff3ddf
80107-001-032023-07-28C16284748780-1d6a99b39-c87b-a426-e053-dadaa90af4c2aa5f8929-2e8e-4d19-8b0c-75eed2ff3ddf
80107-001-042023-07-28C16284748780-1d6a99b39-c87b-a426-e053-dadaa90af4c2aa5f8929-2e8e-4d19-8b0c-75eed2ff3ddf
80107-001-052023-07-28C16284748780-1d6a99b39-c87b-a426-e053-dadaa90af4c2aa5f8929-2e8e-4d19-8b0c-75eed2ff3ddf
80107-001-062023-07-28C16284748780-1d6a99b39-c87b-a426-e053-dadaa90af4c2aa5f8929-2e8e-4d19-8b0c-75eed2ff3ddf
80107-001-012022-03-03C16284748780-1d6a99b39-c87b-a426-e053-dadaa90af4c2aa5f8929-2e8e-4d19-8b0c-75eed2ff3ddf
80107-001-022022-03-03C16284748780-1d6a99b39-c87b-a426-e053-dadaa90af4c2aa5f8929-2e8e-4d19-8b0c-75eed2ff3ddf
80107-001-032022-03-03C16284748780-1d6a99b39-c87b-a426-e053-dadaa90af4c2aa5f8929-2e8e-4d19-8b0c-75eed2ff3ddf
80107-001-042022-03-03C16284748780-1d6a99b39-c87b-a426-e053-dadaa90af4c2aa5f8929-2e8e-4d19-8b0c-75eed2ff3ddf
80107-001-052022-03-03C16284748780-1d6a99b39-c87b-a426-e053-dadaa90af4c2aa5f8929-2e8e-4d19-8b0c-75eed2ff3ddf
80107-001-062022-03-03C16284748780-1d6a99b39-c87b-a426-e053-dadaa90af4c2aa5f8929-2e8e-4d19-8b0c-75eed2ff3ddf
80107-001-012022-01-28C16284748780-1d6a99b39-c87b-a426-e053-dadaa90af4c2aa5f8929-2e8e-4d19-8b0c-75eed2ff3ddf
80107-001-022022-01-28C16284748780-1d6a99b39-c87b-a426-e053-dadaa90af4c2aa5f8929-2e8e-4d19-8b0c-75eed2ff3ddf
80107-001-032022-01-28C16284748780-1d6a99b39-c87b-a426-e053-dadaa90af4c2aa5f8929-2e8e-4d19-8b0c-75eed2ff3ddf
80107-001-042022-01-28C16284748780-1d6a99b39-c87b-a426-e053-dadaa90af4c2aa5f8929-2e8e-4d19-8b0c-75eed2ff3ddf
80107-001-052022-01-28C16284748780-1d6a99b39-c87b-a426-e053-dadaa90af4c2aa5f8929-2e8e-4d19-8b0c-75eed2ff3ddf
80107-001-062022-01-28C16284748780-1d6a99b39-c87b-a426-e053-dadaa90af4c2aa5f8929-2e8e-4d19-8b0c-75eed2ff3ddf

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80107-001-01M MARVEL SANI CARE Instant Hand Sanitizer30 mL in 1 BOTTLEGEL302
80107-001-02M MARVEL SANI CARE Instant Hand Sanitizer60 mL in 1 BOTTLEGEL602
80107-001-03M MARVEL SANI CARE Instant Hand Sanitizer250 mL in 1 BOTTLEGEL2502
80107-001-04M MARVEL SANI CARE Instant Hand Sanitizer500 mL in 1 BOTTLEGEL5002
80107-001-05M MARVEL SANI CARE Instant Hand Sanitizer1000 mL in 1 BOTTLEGEL10002
80107-001-06M MARVEL SANI CARE Instant Hand Sanitizer3785 mL in 1 BOTTLEGEL37852

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80107-001M MARVEL SANI CARE INSTANT HAND SANITIZER (ALCOHOL) GEL [GUANGZHOU TECHIN DEVELOPMENT CO., LTD]2Legacy NDC, 6 package rows20220304_aa5f8929-2e8e-4d19-8b0c-75eed2ff3ddf.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80107-00180107-001-01, 80107-001-02, 80107-001-03, 80107-001-04, 80107-001-05, 80107-001-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
d95cc4af-ce1d-1b71-e053-2995a90a6d0caa5f8929-2e8e-4d19-8b0c-75eed2ff3ddf2022-03-03WarningsExact identifier
spl id: d95cc4af-ce1d-1b71-e053-2995a90a6d0c
spl set id: aa5f8929-2e8e-4d19-8b0c-75eed2ff3ddf

Reported adverse events (FAERS/openFDA)#

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