Hand Sanitizer

Manufacturer
Witty Cosmetics | Stream2Sea
Effective date
2020-05-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:14:57

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ethanol 62% vlv............................................Antiseptic

INDICATIONS & USAGE SECTION

  • help reduce bacteria that can potentially cause diseases
  • for use when soap & water is not available

WARNINGS SECTION

  • For external use only
  • flammable keep away from heat or flame
  • Do not use on children less than 2 months olds on open skin wounds
  • When using this product keep out of eyes, ears and mouth
  • in case of contact with eyes, rinse thoroughly with water
  • Stop use and ask a doctor if irritation or rash occurs

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

  • If swallowed, seek medical help or contact a Poison Control Center.

INACTIVE INGREDIENT SECTION

  • Deionized water, glycerin, eucalyptus globulus leaf oil, camphor, mixed tocopherols (Vitamin E)

DOSAGE & ADMINISTRATION SECTION

2 fl oz (60ml)

OTC - PURPOSE SECTION

  • help reduce bacteria that can potentially cause diseases
  • for use when soap & water is not available

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

620 ml label620 ml label620ml NDC: 78276-223-92

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78276-223-922022-01-28C16284748780-1d6a99b39-3eb1-a426-e053-dadaa90af4c2SDSpart 2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78276-223-92Hand Sanitizer60 mL in 1 BOTTLELIQUID601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78276-223HAND SANITIZER (ALCOHOL) LIQUID [WITTY COSMETICS]1Legacy NDC, 1 package rows20200528_a6932d5f-7439-3cc9-e053-2995a90ad654.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78276-22378276-223-92
69555-062

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT

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
a692ab51-6336-6b9f-e053-2995a90a2b8fa6932d5f-7439-3cc9-e053-2995a90ad6542020-05-26WarningsExact identifier
spl id: a692ab51-6336-6b9f-e053-2995a90a2b8f
spl set id: a6932d5f-7439-3cc9-e053-2995a90ad654

Reported adverse events (FAERS/openFDA)#

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