FDA.reportPublic FDA data

Dermasil Hand Sanitizer Unscented

Manufacturer
Fantasia Beauty LLC | Fujian Haojin Toiletries Co Ltd.
Effective date
2023-10-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:24:39

Label at a glance#

ProductDermasil Hand Sanitizer Unscented
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Apply a dime size amount to hands. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

  • Hand snitizer 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 fire and flame

Do not use

OTC - DO NOT USE SECTION

  • On childern less than 2 months of age.
  • On open skin wounds.

When using this product

OTC - WHEN USING SECTION

  • Keep out of eyes, ears, and mouth. In case of conatct with eyes, rinse thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develops and persists.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, conatct a doctor or Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply a dime size amount to hands. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

SPL UNCLASSIFIED SECTION

Store between 59-86°F. Avoid freezing and excessive heat above 104°F.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water/Aqua/Eau, Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Aloe Barbadensis Extract, Tocopheryl Acetate. 

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Dermasil Hand Sanitizer Unscented

3.4 FL OZ (100 mL)

Package LabelPackage Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76184-0702-22023-10-10C16284748780-1d6a99b39-6747-a426-e053-dadaa90af4c2Dermasil Hand Sanitizer Unscented
76184-0702-22022-01-28C16284748780-1d6a99b39-6747-a426-e053-dadaa90af4c2Dermasil Hand Sanitizer Unscented

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
76184-070276184-0702-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER INTERPOLYMER TYPE A (55000 CPS)59TL3WG5COIACT
TROLAMINE9O3K93S3TKIACT
ALOE VERA LEAFZY81Z83H0XIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
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
52041132-0572-4c52-a3b3-cb56428d090dde74fbcc-38ba-4ffa-a6c6-34ad2dbaa7482023-10-09WarningsExact identifier
spl id: 52041132-0572-4c52-a3b3-cb56428d090d
spl set id: de74fbcc-38ba-4ffa-a6c6-34ad2dbaa748

Reported adverse events (FAERS/openFDA)#

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