Humetec Ocean Hand Sanitizer Mist

Manufacturer
Houston Medical Technologies LLC
Effective date
2022-10-22
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:51:05

Label at a glance#

ProductHumetec Ocean Hand Sanitizer Mist
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

Hand Sanitizer to help reduce bacteria that potentially can cause disease.

Dosage and administration

Spray hands thoroughly with product and allow to dry without wiping Supervise children under 6 years of age when using this product to avoid swallowing  Do not use other than directed.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses:

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease.

Warnings:

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame. May discolor certain fabrics.

Do not use

OTC - DO NOT USE SECTION

In children under 2 months of age, and on open skin wounds.

When using this product

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

if swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Spray hands thoroughly with product and allow to dry without wiping
  • Supervise children under 6 years of age when using this product to avoid swallowing 
  • Do not use other than directed.

Other information

SPL UNCLASSIFIED SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (aqua), Vegetable Glycerin, Fragrance.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label4Label4

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
80178-01380178-013-01

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
WATER059QF0KO0RIACT
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
eb9920f5-629e-8a79-e053-2a95a90aed409f5aebbf-b69e-4027-afdb-efaaf3dd00d22022-10-22WarningsExact identifier
spl id: eb9920f5-629e-8a79-e053-2a95a90aed40
spl set id: 9f5aebbf-b69e-4027-afdb-efaaf3dd00d2

Reported adverse events (FAERS/openFDA)#

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